Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6867 |
|---|---|
| ensemblid | ENSG00000147526.20 |
| hgncid | 11522 |
| symbol | TACC1 |
| name | transforming acidic coiled-coil containing protein 1 |
| refseq_nuc | NM_006283.3 |
| refseq_prot | NP_006274.2 |
| ensembl_nuc | ENST00000317827.9 |
| ensembl_prot | ENSP00000321703.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 38787236 |
| end | 38853028 |
| strand | + |
| ver | v1.2 |
| region | chr8:38787236-38853028 |
| region5000 | chr8:38782236-38858028 |
| regionname0 | TACC1_chr8_38787236_38853028 |
| regionname5000 | TACC1_chr8_38782236_38858028 |
| 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 | 805 | 330 | 77 | 51 | 146 | 15 | 39 | 110 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0002 | 0/0 | 805 | 7 | 2 | 4 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0003 | 0/0 | 805 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0004 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0005 | 0/0 | 805 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0006 | 0/0 | 805 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0007 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0008 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| 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 | 1/0 | 2418 | 213 | 46 | 32 | 102 | 6 | 26 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0002 | 0/0 | 2418 | 65 | 3 | 8 | 39 | 5 | 10 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0003 | 0/1 | 2418 | 22 | 4 | 10 | 1 | 3 | 3 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0004 | 0/0 | 2418 | 20 | 19 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0005 | 0/0 | 2418 | 7 | 2 | 4 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0006 | 0/0 | 2418 | 5 | 5 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0007 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0008 | 0/0 | 2418 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0009 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0010 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0011 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0012 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0013 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0014 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0015 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0016 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| c0017 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 5353 | 84 | 13 | 23 | 35 | 2 | 10 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0002 | 0/0 | 5350 | 40 | 1 | 1 | 25 | 5 | 8 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0003 | 0/0 | 5354 | 26 | 1 | 4 | 13 | 1 | 7 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0004 | 0/0 | 5354 | 23 | 6 | 4 | 10 | 1 | 2 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0005 | 0/0 | 5354 | 19 | 0 | 1 | 15 | 2 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0006 | 0/0 | 5352 | 13 | 1 | 0 | 12 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0007 | 0/0 | 5339 | 11 | 11 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0008 | 0/1 | 5347 | 10 | 1 | 5 | 0 | 1 | 2 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0009 | 0/0 | 5355 | 8 | 1 | 2 | 1 | 1 | 3 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0010 | 0/0 | 5353 | 7 | 0 | 0 | 7 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0011 | 0/0 | 5352 | 7 | 7 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0012 | 0/0 | 5351 | 6 | 0 | 2 | 4 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0013 | 0/0 | 5350 | 5 | 4 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0014 | 0/0 | 5349 | 5 | 5 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0015 | 0/0 | 5350 | 4 | 0 | 0 | 4 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0016 | 0/0 | 5339 | 4 | 3 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0017 | 0/0 | 5352 | 3 | 1 | 1 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0018 | 0/0 | 5352 | 3 | 2 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0019 | 0/0 | 5355 | 3 | 0 | 0 | 1 | 0 | 2 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0020 | 0/0 | 5353 | 3 | 3 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0021 | 0/0 | 5348 | 3 | 2 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0022 | 0/0 | 5352 | 2 | 0 | 2 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0023 | 0/0 | 5353 | 2 | 0 | 1 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0024 | 0/0 | 5353 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0025 | 0/0 | 5355 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0026 | 0/0 | 5353 | 2 | 0 | 1 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0027 | 0/0 | 5348 | 2 | 0 | 1 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0028 | 0/0 | 5347 | 2 | 0 | 1 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0029 | 0/0 | 5352 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0030 | 0/0 | 5351 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0031 | 0/0 | 5354 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0032 | 0/0 | 5351 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0033 | 0/0 | 5354 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0034 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0035 | 0/0 | 5350 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0036 | 0/0 | 5352 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0037 | 0/0 | 5354 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0038 | 0/0 | 5348 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0039 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0040 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0041 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0042 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0043 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0044 | 0/0 | 5348 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0045 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0046 | 0/0 | 5351 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0047 | 0/0 | 5353 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0048 | 0/0 | 5355 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0049 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0050 | 0/0 | 5350 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0051 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0052 | 0/0 | 5354 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0053 | 0/0 | 5354 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0054 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0055 | 0/0 | 5355 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0056 | 0/0 | 5354 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0057 | 0/0 | 5354 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0058 | 0/0 | 5350 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0059 | 0/0 | 5351 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0060 | 0/0 | 5352 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0061 | 0/0 | 5352 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0062 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0063 | 0/0 | 5339 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0064 | 0/0 | 5352 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0065 | 0/0 | 5352 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0066 | 0/0 | 5347 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0067 | 0/0 | 5348 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0068 | 0/0 | 5354 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0069 | 0/0 | 5354 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| t0070 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 18 | 1 | 1 | 13 | 2 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0002 | 0/1 | 5 | 0 | 3 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0003 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0005 | 0/0 | 4 | 0 | 0 | 0 | 4 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| 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 | 1/0 | 2418 | 213 | 46 | 32 | 102 | 6 | 26 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002 | 0/0 | 2418 | 65 | 3 | 8 | 39 | 5 | 10 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0003 | 0/1 | 2418 | 22 | 4 | 10 | 1 | 3 | 3 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0004 | 0/0 | 2418 | 20 | 19 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0006 | 0/0 | 2418 | 5 | 5 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0008 | 0/0 | 2418 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0009 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0011 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0013 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0002c0005 | 0/0 | 2418 | 7 | 2 | 4 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0003c0007 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0003c0010 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0004c0014 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0005c0015 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0006c0016 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0007c0012 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0008c0017 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7770 | 78 | 13 | 19 | 34 | 2 | 9 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0003 | 0/0 | 7771 | 21 | 0 | 1 | 13 | 0 | 7 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0004 | 0/0 | 7771 | 20 | 5 | 3 | 10 | 0 | 2 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0005 | 0/0 | 7771 | 19 | 0 | 1 | 15 | 2 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0007 | 0/0 | 7756 | 11 | 11 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0009 | 0/0 | 7772 | 6 | 0 | 1 | 1 | 1 | 3 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0010 | 0/0 | 7770 | 7 | 0 | 0 | 7 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0015 | 0/0 | 7767 | 4 | 0 | 0 | 4 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0016 | 0/0 | 7756 | 4 | 3 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0017 | 0/0 | 7769 | 3 | 1 | 1 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0018 | 0/0 | 7769 | 3 | 2 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0019 | 0/0 | 7772 | 2 | 0 | 0 | 1 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0022 | 0/0 | 7769 | 2 | 0 | 2 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0023 | 0/0 | 7770 | 2 | 0 | 1 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0024 | 0/0 | 7770 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0025 | 0/0 | 7772 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0031 | 0/0 | 7771 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0033 | 0/0 | 7771 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0034 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0036 | 0/0 | 7769 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0037 | 0/0 | 7771 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0038 | 0/0 | 7765 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0039 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0040 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0041 | 0/0 | 7770 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0042 | 0/0 | 7770 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0043 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0044 | 0/0 | 7765 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0045 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0047 | 0/0 | 7770 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0048 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0049 | 0/0 | 7770 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0051 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0052 | 0/0 | 7771 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0053 | 0/0 | 7771 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0054 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0055 | 0/0 | 7772 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0056 | 0/0 | 7771 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0057 | 0/0 | 7771 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0063 | 0/0 | 7756 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0068 | 0/0 | 7771 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0001t0069 | 0/0 | 7771 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002t0001 | 0/0 | 7770 | 4 | 0 | 3 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002t0002 | 0/0 | 7767 | 38 | 1 | 1 | 23 | 5 | 8 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002t0004 | 0/0 | 7771 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002t0006 | 0/0 | 7769 | 13 | 1 | 0 | 12 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002t0012 | 0/0 | 7768 | 5 | 0 | 2 | 3 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002t0032 | 0/0 | 7768 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002t0035 | 0/0 | 7767 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002t0050 | 0/0 | 7767 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0002t0061 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0003t0008 | 0/1 | 7764 | 10 | 1 | 5 | 0 | 1 | 2 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0003t0021 | 0/0 | 7765 | 3 | 2 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0003t0026 | 0/0 | 7770 | 2 | 0 | 1 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0003t0027 | 0/0 | 7765 | 2 | 0 | 1 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0003t0028 | 0/0 | 7764 | 2 | 0 | 1 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0003t0062 | 0/0 | 7752 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0003t0066 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0003t0067 | 0/0 | 7765 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0004t0011 | 0/0 | 7769 | 7 | 7 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0004t0013 | 0/0 | 7767 | 5 | 4 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0004t0020 | 0/0 | 7770 | 3 | 3 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0004t0029 | 0/0 | 7769 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0004t0059 | 0/0 | 7768 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0004t0060 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0004t0064 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0006t0014 | 0/0 | 7766 | 5 | 5 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0008t0002 | 0/0 | 7767 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0008t0012 | 0/0 | 7768 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0009t0001 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0011t0002 | 0/0 | 7767 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0001c0013t0004 | 0/0 | 7771 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0002c0005t0003 | 0/0 | 7771 | 5 | 1 | 3 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0002c0005t0009 | 0/0 | 7772 | 2 | 1 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0003c0007t0030 | 0/0 | 7768 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0003c0007t0065 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0003c0010t0046 | 0/0 | 7768 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0004c0014t0070 | 0/0 | 7770 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0005c0015t0019 | 0/0 | 7772 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0006c0016t0001 | 0/0 | 7770 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0007c0012t0004 | 0/0 | 7771 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| a0008c0017t0058 | 0/0 | 7767 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | copy fasta | chr8 | 38782236 | 38858028 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0001 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0007g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0009g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0009g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0009g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0010g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0010g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0015g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0015g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0015g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0015g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0016g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0016g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0016g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0017g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0017g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0017g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0018g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0018g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0018g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0019g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0019g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0022g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0022g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0023g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0023g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0024g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0025g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0025g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0031g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0031g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0033g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0034g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0036g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0037g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0038g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0039g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0040g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0041g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0042g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0043g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0044g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0045g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0047g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0048g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0049g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0051g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0052g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0053g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0054g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0055g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0056g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0057g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0063g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0068g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0001t0069g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0005 | 0/0 | 4 | 0 | 0 | 0 | 4 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0012g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0012g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0012g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0012g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0012g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0032g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0035g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0050g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0002t0061g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0008g0002 | 0/1 | 5 | 0 | 3 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0008g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0008g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0008g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0008g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0021g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0021g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0026g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0026g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0027g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0027g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0028g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0028g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0062g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0066g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0003t0067g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0011g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0011g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0011g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0013g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0013g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0013g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0013g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0013g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0020g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0020g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0020g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0029g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0029g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0059g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0060g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0004t0064g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0006t0014g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0006t0014g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0006t0014g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0006t0014g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0008t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0008t0012g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0009t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0011t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0001c0013t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0002c0005t0003g0001 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0002c0005t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0002c0005t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0002c0005t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0002c0005t0009g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0003c0007t0030g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0003c0007t0030g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0003c0007t0065g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0003c0010t0046g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0004c0014t0070g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0005c0015t0019g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0006c0016t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0007c0012t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| a0008c0017t0058g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0028 | g0092 | EUR | GBR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00099 | hp2 | a0002 | c0005 | t0003 | g0001 | EUR | GBR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00140 | hp2 | a0001 | c0003 | t0008 | g0096 | EUR | GBR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00280 | hp1 | a0001 | c0001 | t0009 | g0226 | EUR | FIN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0055 | EUR | FIN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | FIN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0187 | EUR | FIN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00408 | hp1 | a0001 | c0002 | t0006 | g0074 | EAS | CHS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | CHS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | CHS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00438 | hp2 | a0001 | c0002 | t0050 | g0033 | EAS | CHS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00642 | hp1 | a0002 | c0005 | t0009 | g0018 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00733 | hp1 | a0006 | c0016 | t0001 | g0190 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00733 | hp2 | a0001 | c0001 | t0009 | g0227 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00735 | hp2 | a0001 | c0002 | t0004 | g0025 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00738 | hp1 | a0001 | c0001 | t0022 | g0141 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00738 | hp2 | a0002 | c0005 | t0003 | g0007 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01070 | hp1 | a0001 | c0001 | t0018 | g0235 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01074 | hp1 | a0001 | c0001 | t0022 | g0164 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01074 | hp2 | a0001 | c0002 | t0032 | g0026 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01081 | hp2 | a0002 | c0005 | t0003 | g0001 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01106 | hp1 | a0001 | c0002 | t0012 | g0061 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01167 | hp1 | a0001 | c0003 | t0062 | g0093 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01167 | hp2 | a0001 | c0001 | t0016 | g0028 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01168 | hp2 | a0001 | c0003 | t0028 | g0086 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01192 | hp1 | a0001 | c0003 | t0008 | g0084 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01243 | hp1 | a0001 | c0001 | t0017 | g0181 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01243 | hp2 | a0001 | c0003 | t0008 | g0002 | AMR | PUR | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01255 | hp1 | a0001 | c0004 | t0013 | g0263 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01261 | hp1 | a0001 | c0003 | t0026 | g0097 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01346 | hp1 | a0001 | c0001 | t0023 | g0166 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01346 | hp2 | a0001 | c0003 | t0008 | g0088 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01358 | hp1 | a0001 | c0001 | t0047 | g0080 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01358 | hp2 | a0001 | c0002 | t0012 | g0034 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0113 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | IBS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01515 | hp2 | a0001 | c0013 | t0004 | g0241 | EUR | IBS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | IBS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01884 | hp1 | a0001 | c0004 | t0059 | g0280 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01884 | hp2 | a0001 | c0004 | t0013 | g0261 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01891 | hp1 | a0001 | c0004 | t0013 | g0262 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01891 | hp2 | a0001 | c0001 | t0024 | g0031 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01975 | hp2 | a0001 | c0003 | t0021 | g0091 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01978 | hp1 | a0001 | c0003 | t0027 | g0085 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0131 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02004 | hp2 | a0001 | c0003 | t0008 | g0002 | AMR | PEL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02015 | hp1 | a0001 | c0001 | t0052 | g0001 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02027 | hp1 | a0001 | c0002 | t0012 | g0041 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02027 | hp2 | a0001 | c0001 | t0034 | g0135 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0248 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02055 | hp2 | a0003 | c0007 | t0065 | g0229 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02056 | hp1 | a0001 | c0001 | t0033 | g0225 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02083 | hp1 | a0001 | c0003 | t0066 | g0089 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02083 | hp2 | a0001 | c0001 | t0015 | g0221 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02129 | hp1 | a0001 | c0001 | t0056 | g0001 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02132 | hp2 | a0001 | c0001 | t0015 | g0216 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02145 | hp2 | a0002 | c0005 | t0009 | g0003 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | CDX | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | CDX | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02257 | hp1 | a0001 | c0004 | t0013 | g0260 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02257 | hp2 | a0001 | c0004 | t0011 | g0014 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02258 | hp2 | a0001 | c0002 | t0006 | g0051 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02280 | hp1 | a0001 | c0006 | t0014 | g0030 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02280 | hp2 | a0001 | c0004 | t0011 | g0277 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0253 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02602 | hp1 | a0001 | c0003 | t0008 | g0002 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0068 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02622 | hp1 | a0001 | c0001 | t0041 | g0134 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0256 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02630 | hp1 | a0001 | c0006 | t0014 | g0266 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02630 | hp2 | a0001 | c0001 | t0048 | g0142 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02647 | hp1 | a0001 | c0002 | t0061 | g0242 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02647 | hp2 | a0001 | c0006 | t0014 | g0265 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02723 | hp1 | a0007 | c0012 | t0004 | g0083 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02723 | hp2 | a0003 | c0007 | t0030 | g0231 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0193 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02738 | hp2 | a0001 | c0003 | t0027 | g0087 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02818 | hp1 | a0001 | c0004 | t0064 | g0269 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02818 | hp2 | a0001 | c0001 | t0031 | g0115 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02886 | hp1 | a0001 | c0004 | t0020 | g0271 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02895 | hp1 | a0001 | c0004 | t0011 | g0279 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02896 | hp1 | a0001 | c0001 | t0018 | g0150 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02896 | hp2 | a0001 | c0004 | t0011 | g0276 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02897 | hp1 | a0001 | c0004 | t0011 | g0014 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02922 | hp2 | a0001 | c0003 | t0008 | g0109 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02970 | hp1 | a0001 | c0001 | t0063 | g0029 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02970 | hp2 | a0001 | c0004 | t0029 | g0275 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02976 | hp1 | a0004 | c0014 | t0070 | g0082 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0136 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0251 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03130 | hp1 | a0001 | c0004 | t0020 | g0270 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0250 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0028 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03239 | hp1 | a0001 | c0003 | t0008 | g0090 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03453 | hp1 | a0001 | c0004 | t0011 | g0014 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03453 | hp2 | a0001 | c0001 | t0042 | g0158 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03486 | hp1 | a0001 | c0003 | t0021 | g0017 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03486 | hp2 | a0001 | c0004 | t0029 | g0274 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03540 | hp2 | a0001 | c0004 | t0011 | g0278 | AFR | GWD | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03579 | hp1 | a0001 | c0004 | t0020 | g0272 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03579 | hp2 | a0003 | c0010 | t0046 | g0230 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03704 | hp1 | a0001 | c0001 | t0069 | g0008 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0189 | SAS | PJL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0219 | SAS | BEB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03834 | hp1 | a0001 | c0002 | t0035 | g0063 | SAS | BEB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03834 | hp2 | a0001 | c0001 | t0036 | g0146 | SAS | BEB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03927 | hp1 | a0001 | c0001 | t0009 | g0117 | SAS | BEB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0044 | SAS | BEB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04115 | hp2 | a0001 | c0001 | t0009 | g0001 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04184 | hp1 | a0001 | c0001 | t0019 | g0027 | SAS | BEB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04184 | hp2 | a0005 | c0015 | t0019 | g0130 | SAS | BEB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0060 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04199 | hp2 | a0001 | c0001 | t0055 | g0188 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0037 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04204 | hp2 | a0001 | c0001 | t0009 | g0008 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | STU | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0249 | AFR | YRI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18522 | hp2 | a0001 | c0004 | t0060 | g0273 | AFR | YRI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | CHB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18747 | hp2 | a0001 | c0001 | t0045 | g0023 | EAS | CHB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18906 | hp1 | a0001 | c0001 | t0044 | g0170 | AFR | YRI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0254 | AFR | YRI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18942 | hp2 | a0001 | c0009 | t0001 | g0011 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18956 | hp1 | a0001 | c0001 | t0039 | g0032 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18956 | hp2 | a0001 | c0002 | t0006 | g0078 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18959 | hp1 | a0001 | c0001 | t0017 | g0009 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18959 | hp2 | a0001 | c0002 | t0006 | g0075 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18960 | hp1 | a0001 | c0002 | t0006 | g0015 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18962 | hp2 | a0001 | c0001 | t0057 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18965 | hp2 | a0001 | c0008 | t0002 | g0066 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18969 | hp2 | a0001 | c0002 | t0006 | g0015 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18971 | hp2 | a0001 | c0001 | t0040 | g0167 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18972 | hp1 | a0001 | c0001 | t0037 | g0160 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18973 | hp2 | a0001 | c0008 | t0012 | g0004 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18978 | hp1 | a0001 | c0001 | t0010 | g0154 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18979 | hp2 | a0001 | c0002 | t0006 | g0071 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18981 | hp2 | a0001 | c0001 | t0068 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18984 | hp1 | a0001 | c0001 | t0015 | g0215 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18986 | hp2 | a0001 | c0001 | t0051 | g0245 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18987 | hp1 | a0001 | c0001 | t0010 | g0112 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18987 | hp2 | a0001 | c0011 | t0002 | g0040 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18992 | hp2 | a0001 | c0001 | t0043 | g0024 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18994 | hp1 | a0001 | c0001 | t0025 | g0118 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19004 | hp1 | a0001 | c0002 | t0006 | g0070 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0156 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19005 | hp1 | a0001 | c0001 | t0019 | g0012 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19005 | hp2 | a0001 | c0002 | t0012 | g0067 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19007 | hp1 | a0001 | c0001 | t0010 | g0110 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19007 | hp2 | a0001 | c0001 | t0025 | g0007 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19010 | hp1 | a0001 | c0002 | t0006 | g0076 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19011 | hp2 | a0001 | c0002 | t0006 | g0072 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0255 | AFR | LWK | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | LWK | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0259 | AFR | LWK | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19043 | hp2 | a0001 | c0004 | t0013 | g0268 | AFR | LWK | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19056 | hp2 | a0001 | c0001 | t0010 | g0209 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19059 | hp1 | a0001 | c0001 | t0054 | g0116 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19059 | hp2 | a0001 | c0001 | t0015 | g0217 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19060 | hp1 | a0001 | c0001 | t0053 | g0133 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19076 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19076 | hp2 | a0001 | c0002 | t0012 | g0050 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19077 | hp2 | a0001 | c0002 | t0006 | g0079 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19080 | hp1 | a0001 | c0002 | t0006 | g0077 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19083 | hp1 | a0001 | c0001 | t0010 | g0192 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19086 | hp2 | a0001 | c0002 | t0006 | g0073 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19087 | hp1 | a0001 | c0001 | t0010 | g0111 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19090 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19240 | hp1 | a0001 | c0003 | t0021 | g0017 | AFR | YRI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA19240 | hp2 | a0001 | c0001 | t0024 | g0031 | AFR | YRI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20129 | hp1 | a0001 | c0001 | t0031 | g0114 | AFR | ASW | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20129 | hp2 | a0001 | c0003 | t0067 | g0094 | AFR | ASW | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0001 | EUR | TSI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20752 | hp2 | a0001 | c0001 | t0023 | g0210 | EUR | TSI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | TSI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20805 | hp2 | a0001 | c0003 | t0026 | g0095 | EUR | TSI | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0124 | SAS | GIH | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01123 | hp1 | a0002 | c0005 | t0003 | g0018 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG01123 | hp2 | a0001 | c0003 | t0008 | g0002 | AMR | CLM | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02559 | hp1 | a0001 | c0001 | t0038 | g0163 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG02559 | hp2 | a0003 | c0007 | t0030 | g0228 | AFR | ACB | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03471 | hp1 | a0001 | c0006 | t0014 | g0267 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0252 | AFR | MSL | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG06807 | hp1 | a0001 | c0001 | t0049 | g0208 | AFR | USA | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| HG06807 | hp2 | a0002 | c0005 | t0003 | g0001 | AFR | USA | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20300 | hp1 | a0001 | c0006 | t0014 | g0030 | AFR | USA | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA20300 | hp2 | a0001 | c0001 | t0017 | g0180 | AFR | USA | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA21309 | hp1 | a0008 | c0017 | t0058 | g0264 | AFR | LWK | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0008 | g0002 | REF | REF | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0186 | REF | REF | TACC1_chr8_38782236_38858028 | TACC1 | chr8 | 38782236 | 38858028 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38819593
|
C | T | 1 | a0008 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.349C>T | p.Pro117Ser | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 696/7770 | 349/2418 | 117/805 | chr8 | 38819593 | ||
| chr8:38819804
|
C | T | 1 | a0002 | 7 | HG00099.hp2 HG00642.hp1 HG00738.hp2 others(4): Show |
missense_variant | MODERATE | c.560C>T | p.Pro187Leu | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 907/7770 | 560/2418 | 187/805 | chr8 | 38819804 | ||
| chr8:38819972
|
T | C | 1 | a0003 | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
missense_variant | MODERATE | c.728T>C | p.Ile243Thr | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 1075/7770 | 728/2418 | 243/805 | chr8 | 38819972 | ||
| chr8:38820389
|
C | T | 1 | a0004 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1145C>T | p.Ser382Phe | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 1492/7770 | 1145/2418 | 382/805 | chr8 | 38820389 | ||
| chr8:38820440
|
G | A | 1 | a0005 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1196G>A | p.Ser399Asn | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 1543/7770 | 1196/2418 | 399/805 | chr8 | 38820440 | ||
| chr8:38836199
|
C | T | 1 | a0006 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.1751C>T | p.Ser584Leu | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/13 | 2098/7770 | 1751/2418 | 584/805 | chr8 | 38836199 | ||
| chr8:38842318
|
G | T | 1 | a0007 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1992G>T | p.Gln664His | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 10/13 | 2339/7770 | 1992/2418 | 664/805 | chr8 | 38842318 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38787615
|
C | A | 1 | a0001c0008 | 2 | NA18965.hp2 NA18973.hp2 |
synonymous_variant | LOW | c.33C>A | p.Pro11Pro | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/13 | 380/7770 | 33/2418 | 11/805 | chr8 | 38787615 | ||
| chr8:38819724
|
G | A | 1 | a0001c0006 | 5 | HG02280.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
synonymous_variant | LOW | c.480G>A | p.Thr160Thr | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 827/7770 | 480/2418 | 160/805 | chr8 | 38819724 | ||
| chr8:38819901
|
T | C | 1 | a0001c0009 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.657T>C | p.Cys219Cys | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 1004/7770 | 657/2418 | 219/805 | chr8 | 38819901 | ||
| chr8:38819955
|
C | G | 1 | a0006c0016 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.711C>G | p.Pro237Pro | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 1058/7770 | 711/2418 | 237/805 | chr8 | 38819955 | ||
| chr8:38820162
|
G | T | 1 | a0005c0015 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.918G>T | p.Gly306Gly | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 1265/7770 | 918/2418 | 306/805 | chr8 | 38820162 | ||
| chr8:38820414
|
A | G | 4 | a0001c0002a0001c0003a0001c0008others(1): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
synonymous_variant | LOW | c.1170A>G | p.Glu390Glu | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/13 | 1517/7770 | 1170/2418 | 390/805 | chr8 | 38820414 | ||
| chr8:38825347
|
C | T | 1 | a0003c0010 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1431C>T | p.Leu477Leu | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/13 | 1778/7770 | 1431/2418 | 477/805 | chr8 | 38825347 | ||
| chr8:38827335
|
T | C | 11 | a0001c0002a0001c0003a0001c0004others(8): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
synonymous_variant | LOW | c.1620T>C | p.Pro540Pro | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/13 | 1967/7770 | 1620/2418 | 540/805 | chr8 | 38827335 | ||
| chr8:38838478
|
T | C | 4 | a0001c0002a0001c0008a0001c0011others(1): Show | 69 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(66): Show |
synonymous_variant | LOW | c.1848T>C | p.Thr616Thr | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/13 | 2195/7770 | 1848/2418 | 616/805 | chr8 | 38838478 | ||
| chr8:38843381
|
A | G | 1 | a0001c0013 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.2214A>G | p.Glu738Glu | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/13 | 2561/7770 | 2214/2418 | 738/805 | chr8 | 38843381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38787287
|
CG | C | 2 | a0001c0001t0022a0001c0002t0032 | 3 | HG00738.hp1 HG01074.hp1 HG01074.hp2 |
5_prime_UTR_variant | MODIFIER | c.-293delG | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/13 | 293 | INFO_REALIGN_3_PRIME | chr8 | 38787287 | ||||
| chr8:38787321
|
G | A | 1 | a0001c0001t0033 | 1 | HG02056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-262G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/13 | 262 | chr8 | 38787321 | |||||
| chr8:38787396
|
A | G | 33 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(30): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-187A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/13 | 187 | chr8 | 38787396 | |||||
| chr8:38787545
|
C | T | 1 | a0004c0014t0070 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/13 | 38 | chr8 | 38787545 | |||||
| chr8:38787571
|
G | A | 2 | a0001c0001t0025a0001c0001t0057 | 3 | NA18962.hp2 NA18994.hp1 NA19007.hp2 |
5_prime_UTR_variant | MODIFIER | c.-12G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/13 | 12 | chr8 | 38787571 | |||||
| chr8:38848373
|
T | TG | 3 | a0001c0004t0013a0001c0006t0014a0008c0017t0058 | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*354dupG | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 355 | INFO_REALIGN_3_PRIME | chr8 | 38848373 | ||||
| chr8:38848381
|
TCTC | T | 1 | a0001c0001t0015 | 4 | HG02083.hp2 HG02132.hp2 NA18984.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*360_*362delTCC | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 360 | INFO_REALIGN_3_PRIME | chr8 | 38848381 | ||||
| chr8:38848686
|
G | A | 1 | a0001c0001t0034 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*663G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 663 | chr8 | 38848686 | |||||
| chr8:38848695
|
G | A | 3 | a0001c0004t0013a0001c0006t0014a0008c0017t0058 | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*672G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 672 | chr8 | 38848695 | |||||
| chr8:38848851
|
C | T | 18 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(15): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*828C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 828 | chr8 | 38848851 | |||||
| chr8:38848856
|
A | G | 1 | a0001c0002t0050 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 833 | chr8 | 38848856 | |||||
| chr8:38848879
|
G | C | 8 | a0001c0002t0002a0001c0002t0006a0001c0002t0012others(5): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 856 | chr8 | 38848879 | |||||
| chr8:38848961
|
C | CT | 27 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(24): Show | 131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*953dupT | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 954 | INFO_REALIGN_3_PRIME | chr8 | 38848961 | ||||
| chr8:38848961
|
CT | C | 4 | a0001c0001t0017a0001c0001t0036a0001c0002t0032others(1): Show | 6 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*953delT | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 953 | INFO_REALIGN_3_PRIME | chr8 | 38848961 | ||||
| chr8:38849101
|
G | A | 2 | a0001c0001t0010a0001c0001t0037 | 8 | NA18972.hp1 NA18978.hp1 NA18987.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1078G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1078 | chr8 | 38849101 | |||||
| chr8:38849132
|
G | T | 1 | a0001c0003t0066 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1109G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1109 | chr8 | 38849132 | |||||
| chr8:38849185
|
TAA | T | 8 | a0001c0002t0002a0001c0002t0006a0001c0002t0012others(5): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1165_*1166delAA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1165 | INFO_REALIGN_3_PRIME | chr8 | 38849185 | ||||
| chr8:38849190
|
G | A | 1 | a0004c0014t0070 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1167G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1167 | chr8 | 38849190 | |||||
| chr8:38849368
|
C | T | 1 | a0001c0001t0056 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1345C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1345 | chr8 | 38849368 | |||||
| chr8:38849381
|
A | G | 1 | a0001c0001t0047 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1358A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1358 | chr8 | 38849381 | |||||
| chr8:38849480
|
T | C | 2 | a0001c0004t0020a0001c0004t0060 | 4 | HG02886.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1457T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1457 | chr8 | 38849480 | |||||
| chr8:38849500
|
C | T | 1 | a0001c0001t0055 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1477C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1477 | chr8 | 38849500 | |||||
| chr8:38849520
|
T | C | 1 | a0001c0001t0038 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1497T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1497 | chr8 | 38849520 | |||||
| chr8:38849655
|
A | G | 1 | a0001c0001t0024 | 2 | HG01891.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1632A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1632 | chr8 | 38849655 | |||||
| chr8:38849696
|
C | T | 3 | a0003c0007t0030a0003c0007t0065a0003c0010t0046 | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1673C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1673 | chr8 | 38849696 | |||||
| chr8:38849934
|
A | T | 8 | a0001c0002t0002a0001c0002t0006a0001c0002t0012others(5): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1911A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1911 | chr8 | 38849934 | |||||
| chr8:38850017
|
A | G | 6 | a0001c0004t0011a0001c0004t0020a0001c0004t0029others(3): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1994A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 1994 | chr8 | 38850017 | |||||
| chr8:38850043
|
T | TTA | 1 | a0001c0002t0006 | 13 | HG00408.hp1 HG02258.hp2 NA18956.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2023_*2024dupTA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2025 | INFO_REALIGN_3_PRIME | chr8 | 38850043 | ||||
| chr8:38850239
|
C | G | 1 | a0004c0014t0070 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2216C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2216 | chr8 | 38850239 | |||||
| chr8:38850266
|
A | C | 2 | a0001c0003t0027a0001c0003t0028 | 4 | HG00099.hp1 HG01168.hp2 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2243A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2243 | chr8 | 38850266 | |||||
| chr8:38850455
|
G | T | 1 | a0001c0001t0056 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2432G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2432 | chr8 | 38850455 | |||||
| chr8:38850456
|
G | T | 1 | a0001c0001t0056 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2433G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2433 | chr8 | 38850456 | |||||
| chr8:38850561
|
G | A | 1 | a0001c0002t0035 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2538G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2538 | chr8 | 38850561 | |||||
| chr8:38850567
|
G | C | 1 | a0001c0001t0039 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2544G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2544 | chr8 | 38850567 | |||||
| chr8:38850659
|
C | T | 4 | a0001c0001t0031a0001c0004t0013a0001c0006t0014others(1): Show | 13 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2636C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2636 | chr8 | 38850659 | |||||
| chr8:38850775
|
C | CA | 14 | a0001c0001t0004a0001c0001t0009a0001c0001t0019others(11): Show | 41 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2777dupA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2778 | INFO_REALIGN_3_PRIME | chr8 | 38850775 | ||||
| chr8:38850775
|
CA | C | 14 | a0001c0001t0018a0001c0001t0049a0001c0001t0054others(11): Show | 30 | HG01070.hp1 HG01106.hp1 HG01358.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2777delA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2777 | INFO_REALIGN_3_PRIME | chr8 | 38850775 | ||||
| chr8:38850775
|
CAA | C | 12 | a0001c0002t0002a0001c0002t0006a0001c0002t0035others(9): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2776_*2777delAA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2776 | INFO_REALIGN_3_PRIME | chr8 | 38850775 | ||||
| chr8:38850775
|
CAAAA | C | 2 | a0001c0004t0013a0008c0017t0058 | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2774_*2777delAAAA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2774 | INFO_REALIGN_3_PRIME | chr8 | 38850775 | ||||
| chr8:38850775
|
CAAAAA | C | 3 | a0001c0001t0038a0001c0001t0044a0001c0006t0014 | 7 | HG02280.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2773_*2777delAAAA others(1): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2773 | INFO_REALIGN_3_PRIME | chr8 | 38850775 | ||||
| chr8:38850775
|
CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0007a0001c0001t0016a0001c0001t0063others(1): Show | 17 | HG01167.hp1 HG01167.hp2 HG02055.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2764_*2777delAAAA others(10): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2764 | INFO_REALIGN_3_PRIME | chr8 | 38850775 | ||||
| chr8:38850780
|
A | G | 1 | a0001c0001t0069 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2757A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2757 | chr8 | 38850780 | |||||
| chr8:38850789
|
A | C | 1 | a0001c0001t0045 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2766A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2766 | chr8 | 38850789 | |||||
| chr8:38850799
|
A | G | 1 | a0001c0001t0043 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2776A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 2776 | chr8 | 38850799 | |||||
| chr8:38851450
|
G | A | 1 | a0001c0004t0011 | 7 | HG02257.hp2 HG02280.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3427G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 3427 | chr8 | 38851450 | |||||
| chr8:38851592
|
T | G | 1 | a0001c0001t0052 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3569T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 3569 | chr8 | 38851592 | |||||
| chr8:38851752
|
C | T | 1 | a0001c0001t0036 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3729C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 3729 | chr8 | 38851752 | |||||
| chr8:38851884
|
A | G | 3 | a0001c0001t0007a0001c0001t0016a0001c0001t0063 | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3861A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 3861 | chr8 | 38851884 | |||||
| chr8:38851890
|
T | C | 1 | a0001c0001t0053 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3867T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 3867 | chr8 | 38851890 | |||||
| chr8:38851933
|
TTGAC | T | 7 | a0001c0003t0008a0001c0003t0021a0001c0003t0027others(4): Show | 20 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3913_*3916delACTG | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 3913 | INFO_REALIGN_3_PRIME | chr8 | 38851933 | ||||
| chr8:38852035
|
C | T | 18 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(15): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*4012C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4012 | chr8 | 38852035 | |||||
| chr8:38852037
|
C | T | 2 | a0001c0004t0060a0001c0004t0064 | 2 | HG02818.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4014C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4014 | chr8 | 38852037 | |||||
| chr8:38852070
|
G | A | 1 | a0004c0014t0070 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4047G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4047 | chr8 | 38852070 | |||||
| chr8:38852169
|
C | A | 1 | a0001c0001t0023 | 2 | HG01346.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4146C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4146 | chr8 | 38852169 | |||||
| chr8:38852183
|
C | G | 1 | a0001c0001t0042 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4160C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4160 | chr8 | 38852183 | |||||
| chr8:38852301
|
T | C | 1 | a0001c0001t0063 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4278T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4278 | chr8 | 38852301 | |||||
| chr8:38852582
|
A | G | 2 | a0001c0001t0048a0001c0001t0049 | 2 | HG02630.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4559A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4559 | chr8 | 38852582 | |||||
| chr8:38852583
|
G | C | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4560G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4560 | chr8 | 38852583 | |||||
| chr8:38852586
|
C | G | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4563C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4563 | chr8 | 38852586 | |||||
| chr8:38852588
|
G | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4565G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4565 | chr8 | 38852588 | |||||
| chr8:38852589
|
C | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4566C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4566 | chr8 | 38852589 | |||||
| chr8:38852590
|
G | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4567G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4567 | chr8 | 38852590 | |||||
| chr8:38852592
|
G | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4569G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4569 | chr8 | 38852592 | |||||
| chr8:38852593
|
T | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4570T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4570 | chr8 | 38852593 | |||||
| chr8:38852598
|
G | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4575G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4575 | chr8 | 38852598 | |||||
| chr8:38852601
|
C | G | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4578C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4578 | chr8 | 38852601 | |||||
| chr8:38852602
|
A | G | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4579A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4579 | chr8 | 38852602 | |||||
| chr8:38852603
|
C | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4580C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4580 | chr8 | 38852603 | |||||
| chr8:38852605
|
C | G | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4582C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4582 | chr8 | 38852605 | |||||
| chr8:38852606
|
C | G | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4583C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4583 | chr8 | 38852606 | |||||
| chr8:38852611
|
C | G | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4588C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4588 | chr8 | 38852611 | |||||
| chr8:38852612
|
C | T | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4589C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4589 | chr8 | 38852612 | |||||
| chr8:38852613
|
T | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4590T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4590 | chr8 | 38852613 | |||||
| chr8:38852614
|
C | G | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4591C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4591 | chr8 | 38852614 | |||||
| chr8:38852621
|
G | A | 1 | a0008c0017t0058 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4598G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4598 | chr8 | 38852621 | |||||
| chr8:38852626
|
T | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4603T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4603 | chr8 | 38852626 | |||||
| chr8:38852634
|
C | T | 1 | a0001c0001t0016 | 4 | HG01167.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4611C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4611 | chr8 | 38852634 | |||||
| chr8:38852637
|
C | A | 1 | a0001c0001t0040 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4614C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4614 | chr8 | 38852637 | |||||
| chr8:38852732
|
A | G | 1 | a0001c0001t0041 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4709A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 13/13 | 4709 | chr8 | 38852732 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38787985
|
C | G | 1 | a0001c0001t0024g0031 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.161+242C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/12 | chr8 | 38787985 | ||||||
| chr8:38788091
|
C | T | 13 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+348C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/12 | chr8 | 38788091 | ||||||
| chr8:38788136
|
C | G | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.161+393C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/12 | chr8 | 38788136 | ||||||
| chr8:38788240
|
G | A | 1 | a0001c0001t0039g0032 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.162-464G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/12 | chr8 | 38788240 | ||||||
| chr8:38788506
|
G | A | 2 | a0001c0004t0013g0260a0001c0004t0013g0261 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.162-198G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/12 | chr8 | 38788506 | ||||||
| chr8:38788541
|
C | G | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.162-163C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/12 | chr8 | 38788541 | ||||||
| chr8:38788574
|
C | T | 1 | a0001c0002t0002g0259 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-130C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 1/12 | chr8 | 38788574 | ||||||
| chr8:38788884
|
G | A | 53 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(50): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.277+65G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38788884 | ||||||
| chr8:38789003
|
T | C | 1 | a0001c0001t0047g0080 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.277+184T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38789003 | ||||||
| chr8:38789021
|
A | G | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+202A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38789021 | ||||||
| chr8:38789279
|
G | A | 1 | a0001c0001t0005g0081 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.277+460G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38789279 | ||||||
| chr8:38789469
|
A | G | 1 | a0001c0001t0003g0258 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.277+650A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38789469 | ||||||
| chr8:38789550
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.277+731A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38789550 | ||||||
| chr8:38789880
|
C | T | 1 | a0001c0004t0059g0280 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.277+1061C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38789880 | ||||||
| chr8:38790027
|
A | G | 1 | a0001c0002t0006g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.277+1208A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38790027 | ||||||
| chr8:38790368
|
G | A | 5 | a0001c0004t0020g0270a0001c0004t0020g0271a0001c0004t0020g0272others(2): Show | 5 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+1549G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38790368 | ||||||
| chr8:38790403
|
G | T | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.277+1584G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38790403 | ||||||
| chr8:38790527
|
C | T | 13 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+1708C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38790527 | ||||||
| chr8:38790652
|
C | T | 1 | a0001c0001t0004g0247 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.277+1833C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38790652 | ||||||
| chr8:38790705
|
C | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+1886C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38790705 | ||||||
| chr8:38790786
|
A | G | 11 | a0001c0002t0006g0015a0001c0002t0006g0070a0001c0002t0006g0071others(8): Show | 12 | HG00408.hp1 NA18956.hp2 NA18959.hp2 others(9): Show |
intron_variant | MODIFIER | c.277+1967A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38790786 | ||||||
| chr8:38790964
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.277+2145C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38790964 | ||||||
| chr8:38791101
|
T | C | 4 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+2282T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38791101 | ||||||
| chr8:38791106
|
G | T | 1 | a0001c0002t0002g0259 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277+2287G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38791106 | ||||||
| chr8:38791241
|
ACT | A | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+2426_277+2427d others(4): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38791241 | |||||
| chr8:38791308
|
A | G | 4 | a0001c0001t0005g0012a0001c0001t0005g0246a0001c0001t0019g0012others(1): Show | 5 | NA18968.hp1 NA18986.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+2489A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38791308 | ||||||
| chr8:38791362
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.277+2543C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38791362 | ||||||
| chr8:38791444
|
A | G | 1 | a0001c0001t0003g0243 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.277+2625A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38791444 | ||||||
| chr8:38791523
|
G | A | 1 | a0004c0014t0070g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.277+2704G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38791523 | ||||||
| chr8:38791691
|
C | T | 1 | a0001c0002t0002g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.277+2872C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38791691 | ||||||
| chr8:38791873
|
G | T | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.277+3054G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38791873 | ||||||
| chr8:38792336
|
T | A | 3 | a0001c0004t0029g0274a0001c0004t0029g0275a0001c0004t0059g0280 | 3 | HG01884.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.277+3517T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38792336 | ||||||
| chr8:38792551
|
C | T | 1 | a0001c0013t0004g0241 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.277+3732C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38792551 | ||||||
| chr8:38792651
|
G | C | 13 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+3832G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38792651 | ||||||
| chr8:38792672
|
A | G | 8 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0236others(5): Show | 8 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+3853A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38792672 | ||||||
| chr8:38792762
|
G | A | 5 | a0001c0004t0020g0270a0001c0004t0020g0271a0001c0004t0020g0272others(2): Show | 5 | HG02818.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+3943G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38792762 | ||||||
| chr8:38792880
|
G | A | 1 | a0001c0001t0003g0016 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.277+4061G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38792880 | ||||||
| chr8:38793473
|
T | C | 1 | a0007c0012t0004g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.277+4654T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38793473 | ||||||
| chr8:38793553
|
T | A | 15 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(12): Show | 19 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.277+4734T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38793553 | ||||||
| chr8:38793663
|
G | A | 2 | a0001c0004t0013g0260a0001c0004t0013g0261 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.277+4844G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38793663 | ||||||
| chr8:38793882
|
A | G | 3 | a0001c0001t0005g0027a0001c0001t0005g0232a0001c0001t0019g0027 | 3 | HG02155.hp2 HG04184.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.277+5063A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38793882 | ||||||
| chr8:38793891
|
A | G | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+5072A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38793891 | ||||||
| chr8:38794023
|
C | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+5204C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38794023 | ||||||
| chr8:38794195
|
G | T | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.277+5376G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38794195 | ||||||
| chr8:38794207
|
G | T | 1 | a0001c0002t0012g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.277+5388G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38794207 | ||||||
| chr8:38794478
|
T | G | 1 | a0001c0003t0008g0084 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.277+5659T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38794478 | ||||||
| chr8:38794519
|
G | A | 1 | a0001c0002t0050g0033 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.277+5700G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38794519 | ||||||
| chr8:38794546
|
G | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0101others(1): Show | 4 | NA18951.hp1 NA18972.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+5727G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38794546 | ||||||
| chr8:38794554
|
GTGTT | G | 12 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0101others(9): Show | 12 | HG00423.hp2 HG01258.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.277+5743_277+5746d others(6): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38794554 | |||||
| chr8:38794562
|
TTG | T | 111 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(108): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.277+5760_277+5761d others(4): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38794562 | |||||
| chr8:38795231
|
C | T | 2 | a0001c0001t0009g0226a0001c0001t0009g0227 | 2 | HG00280.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.277+6412C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38795231 | ||||||
| chr8:38795596
|
A | G | 4 | a0001c0004t0020g0270a0001c0004t0020g0271a0001c0004t0020g0272others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+6777A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38795596 | ||||||
| chr8:38795735
|
G | A | 1 | a0008c0017t0058g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277+6916G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38795735 | ||||||
| chr8:38795822
|
A | G | 1 | a0001c0001t0009g0227 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.277+7003A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38795822 | ||||||
| chr8:38796026
|
A | G | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+7207A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38796026 | ||||||
| chr8:38796095
|
C | T | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.277+7276C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38796095 | ||||||
| chr8:38796199
|
A | G | 2 | a0001c0002t0002g0064a0001c0002t0002g0065 | 2 | NA18944.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.277+7380A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38796199 | ||||||
| chr8:38797270
|
G | C | 4 | a0001c0006t0014g0030a0001c0006t0014g0265a0001c0006t0014g0266others(1): Show | 5 | HG02280.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+8451G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38797270 | ||||||
| chr8:38797424
|
G | A | 1 | a0001c0004t0059g0280 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.277+8605G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38797424 | ||||||
| chr8:38797439
|
C | G | 13 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+8620C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38797439 | ||||||
| chr8:38797607
|
A | G | 1 | a0001c0002t0035g0063 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.277+8788A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38797607 | ||||||
| chr8:38797610
|
C | G | 1 | a0001c0003t0026g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.277+8791C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38797610 | ||||||
| chr8:38797817
|
C | A | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+8998C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38797817 | ||||||
| chr8:38797841
|
T | C | 15 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(12): Show | 19 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.277+9022T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38797841 | ||||||
| chr8:38797866
|
G | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+9047G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38797866 | ||||||
| chr8:38797901
|
G | A | 3 | a0001c0001t0010g0110a0001c0001t0010g0111a0001c0001t0010g0112 | 3 | NA18987.hp1 NA19007.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.277+9082G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38797901 | ||||||
| chr8:38798020
|
G | A | 1 | a0001c0001t0007g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.277+9201G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38798020 | ||||||
| chr8:38798128
|
C | CT | 22 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(19): Show | 27 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.277+9321dupT | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798128 | |||||
| chr8:38798165
|
C | T | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.277+9346C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38798165 | ||||||
| chr8:38798230
|
C | T | 4 | a0001c0004t0020g0270a0001c0004t0020g0271a0001c0004t0020g0272others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+9411C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38798230 | ||||||
| chr8:38798516
|
C | T | 1 | a0001c0001t0033g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.277+9697C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38798516 | ||||||
| chr8:38798554
|
T | A | 1 | a0001c0001t0004g0113 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.277+9735T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38798554 | ||||||
| chr8:38798606
|
C | CGT | 58 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0024others(55): Show | 63 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.277+9820_277+9821d others(4): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798606 | |||||
| chr8:38798606
|
C | CGTGT | 16 | a0001c0001t0001g0011a0001c0001t0001g0218a0001c0001t0004g0108others(13): Show | 17 | HG01168.hp2 HG01978.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.277+9818_277+9821d others(6): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798606 | |||||
| chr8:38798606
|
C | CGTGTGT | 17 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0007g0029others(14): Show | 17 | HG01255.hp1 HG01261.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.277+9816_277+9821d others(8): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798606 | |||||
| chr8:38798606
|
C | CGTGTGTG others(1): Show |
19 | a0001c0001t0007g0013a0001c0001t0007g0248a0001c0002t0002g0036others(16): Show | 26 | HG00099.hp1 HG01123.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.277+9814_277+9821d others(10): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798606 | |||||
| chr8:38798606
|
C | CGTGTGTG others(3): Show |
38 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(35): Show | 42 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.277+9812_277+9821d others(12): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798606 | |||||
| chr8:38798606
|
C | CGTGTGTG others(5): Show |
8 | a0001c0002t0002g0005a0001c0002t0002g0056a0001c0002t0002g0057others(5): Show | 11 | HG00323.hp1 HG01515.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+9810_277+9821d others(14): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798606 | |||||
| chr8:38798606
|
C | CGTGTGTG others(7): Show |
11 | a0001c0002t0002g0062a0001c0002t0006g0015a0001c0002t0006g0073others(8): Show | 12 | HG00408.hp1 HG00438.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.277+9808_277+9821d others(16): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798606 | |||||
| chr8:38798606
|
CGT | C | 52 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(49): Show | 66 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.277+9820_277+9821d others(4): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798606 | |||||
| chr8:38798606
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0002t0012g0034 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.277+9812_277+9821d others(12): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38798606 | |||||
| chr8:38798608
|
T | C | 1 | a0001c0004t0064g0269 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.277+9789T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38798608 | ||||||
| chr8:38798698
|
G | A | 2 | a0001c0001t0041g0134a0007c0012t0004g0083 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.277+9879G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38798698 | ||||||
| chr8:38798732
|
C | T | 95 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(92): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.277+9913C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38798732 | ||||||
| chr8:38798783
|
G | A | 95 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(92): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.277+9964G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38798783 | ||||||
| chr8:38799134
|
A | G | 55 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(52): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.277+10315A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799134 | ||||||
| chr8:38799262
|
C | T | 1 | a0001c0001t0004g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.277+10443C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799262 | ||||||
| chr8:38799300
|
C | T | 1 | a0001c0003t0026g0095 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.277+10481C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799300 | ||||||
| chr8:38799345
|
C | T | 2 | a0001c0004t0013g0262a0001c0004t0013g0263 | 2 | HG01255.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.277+10526C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799345 | ||||||
| chr8:38799395
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.277+10576C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799395 | ||||||
| chr8:38799462
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.277+10643C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799462 | ||||||
| chr8:38799540
|
A | G | 1 | a0001c0002t0002g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.277+10721A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799540 | ||||||
| chr8:38799777
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.277+10958A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799777 | ||||||
| chr8:38799868
|
A | G | 1 | a0001c0004t0029g0275 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.277+11049A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799868 | ||||||
| chr8:38799925
|
T | G | 1 | a0001c0001t0041g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.277+11106T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38799925 | ||||||
| chr8:38800110
|
G | A | 1 | a0001c0001t0034g0135 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.277+11291G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38800110 | ||||||
| chr8:38800137
|
G | A | 71 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(68): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.277+11318G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38800137 | ||||||
| chr8:38800177
|
C | T | 99 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(96): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.277+11358C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38800177 | ||||||
| chr8:38800213
|
C | A | 1 | a0001c0001t0003g0243 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.277+11394C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38800213 | ||||||
| chr8:38800666
|
A | T | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+11847A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38800666 | ||||||
| chr8:38800787
|
A | G | 2 | a0001c0002t0002g0053a0001c0002t0002g0054 | 2 | HG02523.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.277+11968A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38800787 | ||||||
| chr8:38800876
|
C | A | 40 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(37): Show | 41 | HG00423.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.277+12057C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38800876 | ||||||
| chr8:38801008
|
T | C | 1 | a0003c0007t0030g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.277+12189T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38801008 | ||||||
| chr8:38801012
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02080.hp1 NA18974.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.277+12193G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38801012 | ||||||
| chr8:38801354
|
C | T | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.277+12535C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38801354 | ||||||
| chr8:38801749
|
G | T | 1 | a0008c0017t0058g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277+12930G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38801749 | ||||||
| chr8:38801776
|
T | A | 2 | a0003c0007t0030g0228a0003c0007t0065g0229 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.277+12957T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38801776 | ||||||
| chr8:38801833
|
A | T | 1 | a0004c0014t0070g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.277+13014A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38801833 | ||||||
| chr8:38801916
|
T | G | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+13097T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38801916 | ||||||
| chr8:38802054
|
C | T | 16 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(13): Show | 21 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.277+13235C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38802054 | ||||||
| chr8:38802071
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.277+13252G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38802071 | ||||||
| chr8:38802152
|
C | T | 1 | a0001c0002t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.277+13333C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38802152 | ||||||
| chr8:38802572
|
T | C | 1 | a0001c0002t0002g0069 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.277+13753T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38802572 | ||||||
| chr8:38802611
|
A | T | 13 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+13792A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38802611 | ||||||
| chr8:38802785
|
A | G | 1 | a0001c0001t0053g0133 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.277+13966A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38802785 | ||||||
| chr8:38802930
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.277+14111A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38802930 | ||||||
| chr8:38803053
|
G | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0222a0001c0009t0001g0011 | 4 | NA18942.hp2 NA18983.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+14234G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38803053 | ||||||
| chr8:38803339
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0257 | 2 | NA18963.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.277+14520G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38803339 | ||||||
| chr8:38804293
|
G | A | 1 | a0001c0001t0022g0141 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.278-15229G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38804293 | ||||||
| chr8:38804602
|
G | T | 1 | a0001c0001t0004g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.278-14920G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38804602 | ||||||
| chr8:38805039
|
T | C | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.278-14483T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38805039 | ||||||
| chr8:38805378
|
C | T | 4 | a0001c0002t0006g0072a0001c0002t0006g0076a0001c0002t0006g0077others(1): Show | 4 | NA18956.hp2 NA19010.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-14144C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38805378 | ||||||
| chr8:38805525
|
G | C | 1 | a0001c0003t0008g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.278-13997G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38805525 | ||||||
| chr8:38805575
|
T | C | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-13947T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38805575 | ||||||
| chr8:38805607
|
C | T | 1 | a0001c0002t0006g0078 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.278-13915C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38805607 | ||||||
| chr8:38805709
|
A | G | 1 | a0008c0017t0058g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.278-13813A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38805709 | ||||||
| chr8:38805839
|
G | C | 1 | a0001c0001t0048g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.278-13683G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38805839 | ||||||
| chr8:38805947
|
T | C | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-13575T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38805947 | ||||||
| chr8:38805999
|
A | G | 3 | a0001c0004t0029g0274a0001c0004t0029g0275a0001c0004t0059g0280 | 3 | HG01884.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.278-13523A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38805999 | ||||||
| chr8:38806055
|
G | A | 2 | a0001c0001t0031g0114a0001c0001t0031g0115 | 2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.278-13467G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806055 | ||||||
| chr8:38806178
|
G | T | 1 | a0001c0002t0006g0072 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.278-13344G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806178 | ||||||
| chr8:38806244
|
G | C | 2 | a0001c0001t0004g0102a0001c0001t0004g0108 | 2 | HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.278-13278G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806244 | ||||||
| chr8:38806260
|
G | A | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-13262G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806260 | ||||||
| chr8:38806332
|
T | C | 1 | a0001c0002t0002g0038 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.278-13190T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806332 | ||||||
| chr8:38806432
|
T | C | 1 | a0001c0003t0008g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.278-13090T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806432 | ||||||
| chr8:38806462
|
A | G | 17 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(14): Show | 22 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.278-13060A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806462 | ||||||
| chr8:38806488
|
A | G | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-13034A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806488 | ||||||
| chr8:38806522
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0004g0102a0001c0001t0004g0108 | 3 | HG00423.hp2 NA18975.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.278-13000C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806522 | ||||||
| chr8:38806656
|
G | A | 98 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(95): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.278-12866G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806656 | ||||||
| chr8:38806821
|
T | C | 305 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(302): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.278-12701T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806821 | ||||||
| chr8:38806905
|
G | A | 1 | a0001c0002t0002g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.278-12617G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806905 | ||||||
| chr8:38806966
|
G | A | 53 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(50): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.278-12556G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806966 | ||||||
| chr8:38806967
|
C | T | 71 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(68): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.278-12555C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38806967 | ||||||
| chr8:38807308
|
T | G | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.278-12214T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38807308 | ||||||
| chr8:38807671
|
C | T | 1 | a0001c0001t0003g0258 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.278-11851C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38807671 | ||||||
| chr8:38807779
|
A | G | 1 | a0001c0002t0006g0078 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.278-11743A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38807779 | ||||||
| chr8:38807951
|
G | A | 1 | a0001c0001t0005g0187 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.278-11571G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38807951 | ||||||
| chr8:38808047
|
A | C | 1 | a0001c0002t0002g0052 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.278-11475A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808047 | ||||||
| chr8:38808047
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG01975.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.278-11475A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808047 | ||||||
| chr8:38808098
|
C | T | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-11424C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808098 | ||||||
| chr8:38808126
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.278-11396A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808126 | ||||||
| chr8:38808133
|
G | A | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-11389G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808133 | ||||||
| chr8:38808208
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.278-11314A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808208 | ||||||
| chr8:38808259
|
A | G | 71 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(68): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.278-11263A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808259 | ||||||
| chr8:38808490
|
G | A | 1 | a0001c0001t0004g0247 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.278-11032G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808490 | ||||||
| chr8:38808607
|
G | T | 18 | a0001c0002t0061g0242a0001c0003t0008g0002a0001c0003t0008g0084others(15): Show | 23 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.278-10915G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808607 | ||||||
| chr8:38808663
|
A | T | 17 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(14): Show | 22 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.278-10859A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808663 | ||||||
| chr8:38808681
|
G | A | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-10841G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808681 | ||||||
| chr8:38808696
|
G | A | 1 | a0001c0004t0020g0270 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.278-10826G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808696 | ||||||
| chr8:38808784
|
G | A | 2 | a0001c0002t0002g0259a0001c0002t0012g0034 | 2 | HG01358.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.278-10738G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38808784 | ||||||
| chr8:38809330
|
G | T | 9 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(6): Show | 11 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-10192G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809330 | ||||||
| chr8:38809354
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.278-10168C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809354 | ||||||
| chr8:38809485
|
G | A | 1 | a0006c0016t0001g0190 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.278-10037G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809485 | ||||||
| chr8:38809501
|
G | A | 1 | a0001c0001t0054g0116 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.278-10021G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809501 | ||||||
| chr8:38809502
|
A | G | 1 | a0001c0001t0054g0116 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.278-10020A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809502 | ||||||
| chr8:38809666
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0143others(9): Show | 13 | HG01106.hp2 HG01358.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.278-9856G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809666 | ||||||
| chr8:38809688
|
T | C | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-9834T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809688 | ||||||
| chr8:38809702
|
G | A | 4 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-9820G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809702 | ||||||
| chr8:38809835
|
C | T | 1 | a0001c0001t0054g0116 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.278-9687C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809835 | ||||||
| chr8:38809836
|
T | C | 1 | a0001c0001t0054g0116 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.278-9686T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809836 | ||||||
| chr8:38809962
|
G | A | 4 | a0001c0006t0014g0030a0001c0006t0014g0265a0001c0006t0014g0266others(1): Show | 5 | HG02280.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-9560G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38809962 | ||||||
| chr8:38810154
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.278-9368A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810154 | ||||||
| chr8:38810211
|
A | C | 2 | a0001c0004t0013g0260a0001c0004t0013g0261 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.278-9311A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810211 | ||||||
| chr8:38810408
|
G | A | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-9114G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810408 | ||||||
| chr8:38810555
|
G | A | 71 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(68): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.278-8967G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810555 | ||||||
| chr8:38810564
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 8 | HG01106.hp2 HG01358.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-8958G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810564 | ||||||
| chr8:38810729
|
A | T | 12 | a0001c0002t0006g0015a0001c0002t0006g0051a0001c0002t0006g0070others(9): Show | 13 | HG00408.hp1 HG02258.hp2 NA18956.hp2 others(10): Show |
intron_variant | MODIFIER | c.278-8793A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810729 | ||||||
| chr8:38810801
|
T | C | 99 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(96): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.278-8721T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810801 | ||||||
| chr8:38810876
|
G | A | 71 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(68): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.278-8646G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810876 | ||||||
| chr8:38810974
|
G | C | 1 | a0001c0001t0054g0116 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.278-8548G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810974 | ||||||
| chr8:38810975
|
C | G | 1 | a0001c0001t0054g0116 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.278-8547C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38810975 | ||||||
| chr8:38811067
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0202others(4): Show | 9 | HG01192.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.278-8455G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811067 | ||||||
| chr8:38811176
|
A | T | 10 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(7): Show | 12 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.278-8346A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811176 | ||||||
| chr8:38811177
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.278-8345A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811177 | ||||||
| chr8:38811254
|
CT | C | 305 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(302): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.278-8267delT | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811254 | ||||||
| chr8:38811481
|
A | G | 60 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(57): Show | 68 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.278-8041A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811481 | ||||||
| chr8:38811561
|
A | C | 1 | a0001c0002t0001g0224 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.278-7961A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811561 | ||||||
| chr8:38811562
|
A | G | 4 | a0001c0001t0001g0020a0001c0001t0004g0020a0001c0001t0004g0149others(1): Show | 4 | HG02896.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-7960A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811562 | ||||||
| chr8:38811714
|
A | C | 78 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(75): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.278-7808A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811714 | ||||||
| chr8:38811883
|
C | T | 2 | a0001c0001t0001g0211a0007c0012t0004g0083 | 2 | HG02723.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.278-7639C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811883 | ||||||
| chr8:38811993
|
G | A | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-7529G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38811993 | ||||||
| chr8:38812042
|
T | C | 175 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(172): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.278-7480T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812042 | ||||||
| chr8:38812099
|
A | C | 2 | a0001c0001t0017g0180a0001c0001t0017g0181 | 2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.278-7423A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812099 | ||||||
| chr8:38812127
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.278-7395G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812127 | ||||||
| chr8:38812144
|
A | G | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0018g0136others(1): Show | 4 | HG00639.hp1 HG01070.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-7378A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812144 | ||||||
| chr8:38812211
|
G | A | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-7311G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812211 | ||||||
| chr8:38812298
|
C | G | 15 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(12): Show | 19 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.278-7224C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812298 | ||||||
| chr8:38812383
|
A | T | 1 | a0001c0001t0003g0243 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.278-7139A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812383 | ||||||
| chr8:38812482
|
G | A | 1 | a0001c0001t0009g0117 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.278-7040G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812482 | ||||||
| chr8:38812500
|
G | A | 1 | a0001c0001t0004g0191 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.278-7022G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812500 | ||||||
| chr8:38812797
|
T | G | 3 | a0001c0004t0029g0274a0001c0004t0029g0275a0001c0004t0059g0280 | 3 | HG01884.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.278-6725T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38812797 | ||||||
| chr8:38813025
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0004g0021 | 2 | NA18966.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.278-6497T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813025 | ||||||
| chr8:38813124
|
T | C | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-6398T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813124 | ||||||
| chr8:38813204
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.278-6318G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813204 | ||||||
| chr8:38813289
|
G | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0220a0001c0001t0001g0222others(1): Show | 5 | HG02135.hp1 NA18942.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-6233G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813289 | ||||||
| chr8:38813437
|
C | T | 2 | a0001c0004t0013g0260a0001c0004t0013g0261 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.278-6085C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813437 | ||||||
| chr8:38813675
|
G | A | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-5847G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813675 | ||||||
| chr8:38813773
|
G | A | 1 | a0001c0001t0015g0215 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.278-5749G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813773 | ||||||
| chr8:38813819
|
T | C | 1 | a0001c0002t0002g0056 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.278-5703T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813819 | ||||||
| chr8:38813828
|
T | C | 1 | a0004c0014t0070g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.278-5694T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813828 | ||||||
| chr8:38813849
|
C | T | 1 | a0001c0002t0012g0050 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.278-5673C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813849 | ||||||
| chr8:38813904
|
G | A | 3 | a0001c0006t0014g0030a0001c0006t0014g0265a0001c0006t0014g0266 | 4 | HG02280.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-5618G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38813904 | ||||||
| chr8:38814209
|
T | C | 1 | a0001c0001t0007g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.278-5313T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38814209 | ||||||
| chr8:38814219
|
A | G | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.278-5303A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38814219 | ||||||
| chr8:38814259
|
C | T | 1 | a0001c0001t0004g0179 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.278-5263C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38814259 | ||||||
| chr8:38814366
|
C | T | 1 | a0001c0004t0011g0279 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.278-5156C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38814366 | ||||||
| chr8:38814375
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.278-5147G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38814375 | ||||||
| chr8:38814376
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.278-5146C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38814376 | ||||||
| chr8:38814600
|
G | T | 1 | a0004c0014t0070g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.278-4922G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38814600 | ||||||
| chr8:38814647
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.278-4875G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38814647 | ||||||
| chr8:38815008
|
T | C | 1 | a0001c0001t0039g0032 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.278-4514T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815008 | ||||||
| chr8:38815061
|
G | A | 1 | a0007c0012t0004g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.278-4461G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815061 | ||||||
| chr8:38815103
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0199a0001c0001t0043g0024 | 3 | NA18980.hp1 NA18992.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.278-4419C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815103 | ||||||
| chr8:38815273
|
C | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-4249C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815273 | ||||||
| chr8:38815412
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.278-4110A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815412 | ||||||
| chr8:38815431
|
G | T | 163 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(160): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.278-4091G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815431 | ||||||
| chr8:38815522
|
C | T | 3 | a0001c0001t0016g0028a0001c0001t0016g0249a0001c0001t0016g0251 | 4 | HG01167.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-4000C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815522 | ||||||
| chr8:38815523
|
G | A | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.278-3999G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815523 | ||||||
| chr8:38815638
|
C | T | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.278-3884C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815638 | ||||||
| chr8:38815665
|
C | T | 1 | a0001c0004t0011g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.278-3857C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815665 | ||||||
| chr8:38815666
|
G | A | 3 | a0001c0002t0002g0005a0001c0002t0002g0036a0001c0002t0012g0061 | 6 | HG00323.hp1 HG01106.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-3856G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815666 | ||||||
| chr8:38815671
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0002t0002g0068 | 3 | HG02602.hp2 HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.278-3851G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815671 | ||||||
| chr8:38815850
|
G | A | 1 | a0001c0001t0004g0148 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.278-3672G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38815850 | ||||||
| chr8:38816358
|
A | G | 1 | a0001c0004t0011g0277 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.278-3164A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38816358 | ||||||
| chr8:38816410
|
A | G | 1 | a0001c0004t0013g0261 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.278-3112A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38816410 | ||||||
| chr8:38816546
|
G | A | 55 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(52): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.278-2976G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38816546 | ||||||
| chr8:38817087
|
C | T | 1 | a0001c0001t0003g0258 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.278-2435C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817087 | ||||||
| chr8:38817169
|
A | T | 1 | a0001c0001t0054g0116 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.278-2353A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817169 | ||||||
| chr8:38817189
|
CATT | C | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-2332_278-2330d others(5): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817189 | ||||||
| chr8:38817201
|
A | G | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-2321A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817201 | ||||||
| chr8:38817345
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.278-2177C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817345 | ||||||
| chr8:38817371
|
C | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0143others(9): Show | 13 | HG01106.hp2 HG01358.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.278-2151C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817371 | ||||||
| chr8:38817538
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0004g0177 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.278-1984A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817538 | ||||||
| chr8:38817916
|
C | T | 4 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(1): Show | 6 | HG02257.hp2 HG02280.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-1606C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817916 | ||||||
| chr8:38817919
|
T | TA | 52 | a0001c0001t0001g0010a0001c0001t0001g0098a0001c0001t0001g0099others(49): Show | 54 | HG00423.hp2 HG00642.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.278-1575dupA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38817919 | |||||
| chr8:38817919
|
T | TAA | 8 | a0001c0001t0001g0137a0001c0001t0001g0151a0001c0001t0001g0203others(5): Show | 8 | HG01109.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-1576_278-1575d others(4): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38817919 | |||||
| chr8:38817919
|
T | TTA | 4 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(1): Show | 6 | HG02257.hp2 HG02280.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-1603_278-1602i others(4): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817919 | ||||||
| chr8:38817919
|
TA | T | 97 | a0001c0001t0003g0001a0001c0001t0003g0007a0001c0001t0003g0008others(94): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.278-1575delA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38817919 | |||||
| chr8:38817919
|
TAA | T | 16 | a0001c0001t0016g0028a0001c0001t0016g0249a0001c0001t0016g0251others(13): Show | 22 | HG00099.hp1 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.278-1576_278-1575d others(4): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 38817919 | |||||
| chr8:38817920
|
A | T | 1 | a0001c0004t0029g0275 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.278-1602A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817920 | ||||||
| chr8:38817921
|
A | T | 5 | a0001c0004t0011g0278a0001c0004t0029g0274a0001c0004t0059g0280others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-1601A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817921 | ||||||
| chr8:38817936
|
A | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0143a0001c0001t0001g0144others(3): Show | 7 | HG01106.hp2 HG01358.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-1586A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817936 | ||||||
| chr8:38817989
|
T | G | 1 | a0001c0001t0031g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.278-1533T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38817989 | ||||||
| chr8:38818277
|
C | G | 9 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(6): Show | 11 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-1245C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38818277 | ||||||
| chr8:38818455
|
C | T | 1 | a0004c0014t0070g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.278-1067C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38818455 | ||||||
| chr8:38818533
|
C | G | 1 | a0001c0002t0002g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.278-989C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38818533 | ||||||
| chr8:38818765
|
C | G | 1 | a0001c0003t0067g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.278-757C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38818765 | ||||||
| chr8:38818797
|
T | C | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-725T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38818797 | ||||||
| chr8:38818923
|
G | A | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.278-599G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38818923 | ||||||
| chr8:38818970
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.278-552G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38818970 | ||||||
| chr8:38818994
|
TCTCAATC others(5): Show |
T | 1 | a0001c0001t0054g0116 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.278-527_278-516del others(12): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38818994 | ||||||
| chr8:38819207
|
T | A | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-315T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38819207 | ||||||
| chr8:38819303
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.278-219A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38819303 | ||||||
| chr8:38819467
|
A | C | 1 | a0007c0012t0004g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.278-55A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 2/12 | chr8 | 38819467 | ||||||
| chr8:38820651
|
C | T | 1 | a0001c0006t0014g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1391+16C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38820651 | ||||||
| chr8:38820959
|
A | G | 77 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(74): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1391+324A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38820959 | ||||||
| chr8:38821202
|
CA | C | 14 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(11): Show | 17 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1391+580delA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 38821202 | |||||
| chr8:38821231
|
G | C | 1 | a0001c0004t0029g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1391+596G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38821231 | ||||||
| chr8:38821550
|
A | G | 11 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0101others(8): Show | 11 | HG00423.hp2 HG01258.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.1391+915A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38821550 | ||||||
| chr8:38821560
|
T | G | 1 | a0001c0001t0039g0032 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1391+925T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38821560 | ||||||
| chr8:38821773
|
G | A | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1391+1138G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38821773 | ||||||
| chr8:38821953
|
G | C | 2 | a0001c0001t0001g0162a0001c0001t0004g0179 | 2 | HG02129.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1391+1318G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38821953 | ||||||
| chr8:38822046
|
C | T | 1 | a0001c0003t0008g0096 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1391+1411C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822046 | ||||||
| chr8:38822055
|
A | C | 1 | a0001c0004t0013g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1391+1420A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822055 | ||||||
| chr8:38822085
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1391+1450A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822085 | ||||||
| chr8:38822088
|
T | C | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1391+1453T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822088 | ||||||
| chr8:38822245
|
T | TA | 209 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(206): Show | 229 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1391+1631dupA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 38822245 | |||||
| chr8:38822245
|
T | TAA | 6 | a0001c0001t0001g0098a0001c0001t0001g0184a0001c0001t0001g0185others(3): Show | 6 | HG01975.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391+1630_1391+163 others(6): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 38822245 | |||||
| chr8:38822245
|
TA | T | 6 | a0001c0001t0005g0123a0001c0001t0005g0232a0001c0003t0062g0093others(3): Show | 8 | HG01167.hp1 HG02155.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1391+1631delA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 38822245 | |||||
| chr8:38822264
|
A | G | 1 | a0001c0001t0003g0132 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1391+1629A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822264 | ||||||
| chr8:38822266
|
A | G | 56 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(53): Show | 70 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1391+1631A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822266 | ||||||
| chr8:38822371
|
C | A | 16 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(13): Show | 21 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1391+1736C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822371 | ||||||
| chr8:38822372
|
A | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1391+1737A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822372 | ||||||
| chr8:38822499
|
C | T | 1 | a0004c0014t0070g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1391+1864C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822499 | ||||||
| chr8:38822587
|
A | C | 2 | a0001c0001t0001g0162a0001c0001t0004g0179 | 2 | HG02129.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1391+1952A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822587 | ||||||
| chr8:38822649
|
A | G | 1 | a0001c0004t0013g0262 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1391+2014A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822649 | ||||||
| chr8:38822810
|
G | A | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1391+2175G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822810 | ||||||
| chr8:38822865
|
C | A | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1391+2230C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38822865 | ||||||
| chr8:38823098
|
A | G | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1392-2210A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823098 | ||||||
| chr8:38823103
|
T | C | 13 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1392-2205T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823103 | ||||||
| chr8:38823108
|
G | A | 1 | a0004c0014t0070g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1392-2200G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823108 | ||||||
| chr8:38823131
|
C | T | 1 | a0001c0001t0022g0141 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1392-2177C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823131 | ||||||
| chr8:38823207
|
C | G | 1 | a0001c0002t0050g0033 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1392-2101C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823207 | ||||||
| chr8:38823404
|
C | T | 2 | a0001c0004t0013g0260a0001c0004t0013g0261 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1392-1904C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823404 | ||||||
| chr8:38823558
|
G | A | 18 | a0001c0002t0061g0242a0001c0003t0008g0002a0001c0003t0008g0084others(15): Show | 23 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.1392-1750G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823558 | ||||||
| chr8:38823564
|
C | T | 1 | a0001c0002t0006g0076 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1392-1744C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823564 | ||||||
| chr8:38823658
|
A | G | 3 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229 | 3 | HG02055.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1392-1650A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823658 | ||||||
| chr8:38823713
|
G | A | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1392-1595G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823713 | ||||||
| chr8:38823714
|
C | G | 9 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG00408.hp2 HG02080.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.1392-1594C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823714 | ||||||
| chr8:38823809
|
A | G | 13 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1392-1499A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38823809 | ||||||
| chr8:38824239
|
T | A | 3 | a0001c0001t0001g0020a0001c0001t0004g0020a0001c0001t0004g0149 | 3 | HG02922.hp1 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1392-1069T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38824239 | ||||||
| chr8:38824508
|
A | G | 3 | a0001c0001t0003g0008a0001c0001t0009g0008a0001c0001t0069g0008 | 3 | HG01109.hp2 HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1392-800A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38824508 | ||||||
| chr8:38824512
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0161a0001c0001t0001g0174others(3): Show | 6 | HG00408.hp2 NA18962.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1392-796C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38824512 | ||||||
| chr8:38824686
|
A | G | 1 | a0001c0001t0036g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1392-622A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38824686 | ||||||
| chr8:38824723
|
G | A | 7 | a0001c0001t0016g0028a0001c0001t0016g0249a0001c0001t0016g0251others(4): Show | 8 | HG01167.hp2 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1392-585G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38824723 | ||||||
| chr8:38825013
|
T | C | 96 | a0001c0001t0007g0252a0001c0002t0001g0025a0001c0002t0001g0026others(93): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1392-295T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38825013 | ||||||
| chr8:38825171
|
C | T | 1 | a0001c0006t0014g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1392-137C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 3/12 | chr8 | 38825171 | ||||||
| chr8:38825811
|
T | G | 56 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(53): Show | 70 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1452+443T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38825811 | ||||||
| chr8:38825867
|
C | T | 1 | a0001c0001t0010g0112 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1452+499C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38825867 | ||||||
| chr8:38825897
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0206 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1452+529A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38825897 | ||||||
| chr8:38826005
|
G | A | 1 | a0001c0003t0008g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1452+637G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38826005 | ||||||
| chr8:38826039
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0018g0235 | 2 | HG00642.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1452+671G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38826039 | ||||||
| chr8:38826218
|
A | G | 175 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(172): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1452+850A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38826218 | ||||||
| chr8:38826256
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0004g0193 | 2 | HG01109.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1452+888A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38826256 | ||||||
| chr8:38826335
|
A | C | 1 | a0003c0010t0046g0230 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1453-833A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38826335 | ||||||
| chr8:38826525
|
TAAAG | T | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-639_1453-636d others(6): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 38826525 | |||||
| chr8:38826710
|
A | G | 5 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1453-458A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38826710 | ||||||
| chr8:38826735
|
G | A | 3 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229 | 3 | HG02055.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1453-433G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38826735 | ||||||
| chr8:38826909
|
G | T | 109 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(106): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1453-259G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38826909 | ||||||
| chr8:38826963
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1453-205A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38826963 | ||||||
| chr8:38827145
|
A | G | 1 | a0001c0001t0005g0131 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1453-23A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 4/12 | chr8 | 38827145 | ||||||
| chr8:38827492
|
T | G | 1 | a0001c0001t0003g0124 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1660+117T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38827492 | ||||||
| chr8:38827694
|
G | C | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1660+319G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38827694 | ||||||
| chr8:38827756
|
T | G | 56 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(53): Show | 70 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1660+381T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38827756 | ||||||
| chr8:38827759
|
A | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1660+384A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38827759 | ||||||
| chr8:38827780
|
A | G | 96 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(93): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1660+405A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38827780 | ||||||
| chr8:38827985
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1660+610C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38827985 | ||||||
| chr8:38828083
|
A | G | 53 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(50): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1660+708A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828083 | ||||||
| chr8:38828096
|
A | G | 4 | a0001c0001t0007g0029a0001c0001t0007g0254a0001c0001t0007g0256others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1660+721A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828096 | ||||||
| chr8:38828287
|
T | G | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1660+912T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828287 | ||||||
| chr8:38828321
|
A | G | 5 | a0001c0001t0005g0012a0001c0001t0005g0122a0001c0001t0005g0246others(2): Show | 6 | HG02071.hp2 NA18968.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1660+946A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828321 | ||||||
| chr8:38828527
|
G | A | 164 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(161): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1660+1152G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828527 | ||||||
| chr8:38828549
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1660+1174T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828549 | ||||||
| chr8:38828598
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1660+1223A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828598 | ||||||
| chr8:38828617
|
C | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | NA18962.hp1 NA18968.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1660+1242C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828617 | ||||||
| chr8:38828850
|
C | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1660+1475C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828850 | ||||||
| chr8:38828851
|
A | G | 1 | a0001c0002t0002g0037 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1660+1476A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828851 | ||||||
| chr8:38828853
|
G | C | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1660+1478G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38828853 | ||||||
| chr8:38829644
|
C | T | 1 | a0001c0002t0002g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1661-1481C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38829644 | ||||||
| chr8:38829712
|
T | C | 174 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(171): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1661-1413T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38829712 | ||||||
| chr8:38830335
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1661-790C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38830335 | ||||||
| chr8:38830454
|
T | C | 91 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(88): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1661-671T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38830454 | ||||||
| chr8:38830568
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1661-557T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38830568 | ||||||
| chr8:38830627
|
CAAGG | C | 13 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(10): Show | 17 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1661-494_1661-491d others(6): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 38830627 | |||||
| chr8:38830867
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1661-258G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38830867 | ||||||
| chr8:38830956
|
T | G | 1 | a0001c0001t0005g0189 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1661-169T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 5/12 | chr8 | 38830956 | ||||||
| chr8:38831211
|
C | G | 1 | a0001c0001t0001g0172 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1713+34C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831211 | ||||||
| chr8:38831229
|
TG | T | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+53delG | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831229 | ||||||
| chr8:38831500
|
A | G | 60 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(57): Show | 68 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1713+323A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831500 | ||||||
| chr8:38831719
|
C | G | 1 | a0001c0001t0007g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1713+542C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831719 | ||||||
| chr8:38831748
|
C | T | 1 | a0001c0004t0013g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1713+571C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831748 | ||||||
| chr8:38831771
|
C | T | 1 | a0001c0001t0041g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1713+594C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831771 | ||||||
| chr8:38831809
|
CT | C | 54 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(51): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1713+646delT | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 38831809 | |||||
| chr8:38831831
|
A | C | 3 | a0001c0001t0001g0151a0001c0001t0001g0204a0001c0001t0001g0206 | 3 | HG02965.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1713+654A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831831 | ||||||
| chr8:38831930
|
C | G | 2 | a0001c0001t0041g0134a0007c0012t0004g0083 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1713+753C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831930 | ||||||
| chr8:38831930
|
C | T | 1 | a0001c0001t0003g0121 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1713+753C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831930 | ||||||
| chr8:38831958
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1713+781C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38831958 | ||||||
| chr8:38832238
|
G | A | 1 | a0001c0002t0002g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1713+1061G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38832238 | ||||||
| chr8:38832337
|
G | A | 1 | a0001c0002t0012g0034 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1713+1160G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38832337 | ||||||
| chr8:38832401
|
T | C | 3 | a0001c0006t0014g0030a0001c0006t0014g0265a0001c0006t0014g0266 | 4 | HG02280.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+1224T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38832401 | ||||||
| chr8:38832444
|
C | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1713+1267C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38832444 | ||||||
| chr8:38832595
|
T | G | 1 | a0001c0001t0005g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1713+1418T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38832595 | ||||||
| chr8:38832596
|
C | T | 1 | a0001c0001t0005g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1713+1419C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38832596 | ||||||
| chr8:38832766
|
G | C | 1 | a0001c0001t0033g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1713+1589G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38832766 | ||||||
| chr8:38832798
|
G | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1713+1621G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38832798 | ||||||
| chr8:38832939
|
G | A | 109 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(106): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1713+1762G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38832939 | ||||||
| chr8:38833095
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG01975.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1713+1918C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833095 | ||||||
| chr8:38833148
|
A | G | 2 | a0001c0001t0005g0120a0001c0001t0054g0116 | 2 | NA18949.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.1713+1971A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833148 | ||||||
| chr8:38833214
|
T | C | 1 | a0001c0001t0004g0247 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1713+2037T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833214 | ||||||
| chr8:38833330
|
C | T | 1 | a0001c0001t0003g0132 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1713+2153C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833330 | ||||||
| chr8:38833366
|
T | C | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1713+2189T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833366 | ||||||
| chr8:38833463
|
A | T | 1 | a0001c0002t0012g0050 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1713+2286A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833463 | ||||||
| chr8:38833518
|
T | C | 1 | a0001c0001t0005g0125 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1713+2341T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833518 | ||||||
| chr8:38833621
|
A | G | 96 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(93): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1713+2444A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833621 | ||||||
| chr8:38833768
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1714-2394C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833768 | ||||||
| chr8:38833802
|
G | A | 1 | a0001c0003t0067g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1714-2360G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833802 | ||||||
| chr8:38833871
|
A | G | 2 | a0001c0004t0060g0273a0001c0004t0064g0269 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1714-2291A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38833871 | ||||||
| chr8:38834012
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1714-2150A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38834012 | ||||||
| chr8:38834053
|
A | G | 1 | a0001c0001t0004g0113 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1714-2109A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38834053 | ||||||
| chr8:38834379
|
G | T | 1 | a0001c0002t0006g0071 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1714-1783G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38834379 | ||||||
| chr8:38834750
|
G | A | 16 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(13): Show | 21 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1714-1412G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38834750 | ||||||
| chr8:38834817
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1714-1345A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38834817 | ||||||
| chr8:38834949
|
A | G | 1 | a0001c0001t0018g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1714-1213A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38834949 | ||||||
| chr8:38834980
|
G | A | 2 | a0001c0001t0017g0180a0001c0001t0017g0181 | 2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1714-1182G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38834980 | ||||||
| chr8:38835060
|
T | C | 2 | a0001c0001t0017g0180a0001c0001t0017g0181 | 2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1714-1102T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835060 | ||||||
| chr8:38835080
|
C | T | 1 | a0001c0002t0002g0059 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1714-1082C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835080 | ||||||
| chr8:38835111
|
G | A | 3 | a0001c0002t0002g0069a0001c0002t0012g0050a0004c0014t0070g0082 | 3 | HG02976.hp1 HG03490.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1714-1051G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835111 | ||||||
| chr8:38835115
|
G | A | 2 | a0001c0001t0022g0141a0001c0001t0022g0164 | 2 | HG00738.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1714-1047G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835115 | ||||||
| chr8:38835171
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0018g0136 | 3 | HG00639.hp1 HG01070.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1714-991G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835171 | ||||||
| chr8:38835198
|
G | A | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1714-964G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835198 | ||||||
| chr8:38835253
|
CA | C | 12 | a0001c0001t0001g0233a0001c0001t0054g0116a0001c0004t0011g0014others(9): Show | 14 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1714-893delA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 38835253 | |||||
| chr8:38835572
|
A | G | 1 | a0001c0001t0005g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1714-590A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835572 | ||||||
| chr8:38835617
|
C | T | 18 | a0001c0002t0061g0242a0001c0003t0008g0002a0001c0003t0008g0084others(15): Show | 23 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.1714-545C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835617 | ||||||
| chr8:38835729
|
T | G | 2 | a0001c0001t0001g0178a0001c0001t0004g0177 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1714-433T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835729 | ||||||
| chr8:38835744
|
A | G | 103 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(100): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1714-418A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835744 | ||||||
| chr8:38835863
|
T | C | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1714-299T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 6/12 | chr8 | 38835863 | ||||||
| chr8:38836493
|
T | A | 1 | a0001c0001t0001g0165 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1839+206T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38836493 | ||||||
| chr8:38836571
|
T | C | 1 | a0001c0001t0023g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1839+284T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38836571 | ||||||
| chr8:38836706
|
C | T | 1 | a0005c0015t0019g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1839+419C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38836706 | ||||||
| chr8:38836865
|
T | G | 174 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(171): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1839+578T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38836865 | ||||||
| chr8:38836902
|
G | C | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1839+615G>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38836902 | ||||||
| chr8:38836944
|
G | GT | 13 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1839+665dupT | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 38836944 | |||||
| chr8:38836991
|
C | T | 1 | a0001c0003t0021g0017 | 2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1839+704C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38836991 | ||||||
| chr8:38837105
|
C | CT | 70 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0098others(67): Show | 76 | HG00423.hp2 HG00639.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.1839+837dupT | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 38837105 | |||||
| chr8:38837105
|
CT | C | 8 | a0001c0001t0001g0022a0001c0001t0004g0148a0001c0001t0005g0125others(5): Show | 9 | HG00140.hp1 HG00735.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1839+837delT | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 38837105 | |||||
| chr8:38837197
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1839+910C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38837197 | ||||||
| chr8:38837252
|
T | TA | 91 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(88): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1839+979dupA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 38837252 | |||||
| chr8:38837266
|
A | T | 1 | a0001c0001t0005g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1839+979A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38837266 | ||||||
| chr8:38837284
|
G | A | 1 | a0005c0015t0019g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1839+997G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38837284 | ||||||
| chr8:38837394
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1840-1076A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38837394 | ||||||
| chr8:38837432
|
A | T | 16 | a0001c0003t0008g0002a0001c0003t0008g0084a0001c0003t0008g0088others(13): Show | 21 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1840-1038A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38837432 | ||||||
| chr8:38837459
|
C | T | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1840-1011C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38837459 | ||||||
| chr8:38837528
|
C | T | 1 | a0001c0001t0049g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1840-942C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38837528 | ||||||
| chr8:38838204
|
C | A | 3 | a0001c0001t0001g0022a0001c0001t0023g0166a0001c0001t0023g0210 | 4 | HG00140.hp1 HG00735.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1840-266C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38838204 | ||||||
| chr8:38838277
|
G | A | 3 | a0001c0001t0001g0211a0001c0001t0004g0207a0001c0001t0040g0167 | 3 | NA18951.hp2 NA18971.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1840-193G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38838277 | ||||||
| chr8:38838382
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0168 | 2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1840-88G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 7/12 | chr8 | 38838382 | ||||||
| chr8:38838902
|
C | CT | 15 | a0001c0001t0005g0120a0001c0002t0002g0049a0001c0004t0011g0014others(12): Show | 17 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1916+368dupT | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 38838902 | |||||
| chr8:38838930
|
T | A | 1 | a0001c0003t0008g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1916+384T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38838930 | ||||||
| chr8:38839036
|
A | ACAGGCAT others(25): Show |
1 | a0001c0001t0005g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1916+509_1916+510i others(34): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 38839036 | |||||
| chr8:38839181
|
G | A | 4 | a0001c0001t0010g0110a0001c0001t0010g0111a0001c0001t0010g0112others(1): Show | 4 | NA18987.hp1 NA19004.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1916+635G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839181 | ||||||
| chr8:38839242
|
C | T | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1916+696C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839242 | ||||||
| chr8:38839350
|
A | G | 71 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(68): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1916+804A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839350 | ||||||
| chr8:38839371
|
G | A | 2 | a0001c0004t0013g0262a0001c0004t0013g0263 | 2 | HG01255.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1916+825G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839371 | ||||||
| chr8:38839400
|
C | G | 13 | a0001c0001t0007g0013a0001c0001t0007g0029a0001c0001t0007g0248others(10): Show | 16 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1917-824C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839400 | ||||||
| chr8:38839506
|
G | T | 1 | a0004c0014t0070g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1917-718G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839506 | ||||||
| chr8:38839593
|
G | T | 1 | a0001c0001t0004g0105 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1917-631G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839593 | ||||||
| chr8:38839664
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1917-560C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839664 | ||||||
| chr8:38839665
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0018g0136 | 3 | HG00639.hp1 HG01070.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1917-559G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839665 | ||||||
| chr8:38839683
|
A | G | 1 | a0001c0002t0002g0048 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1917-541A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839683 | ||||||
| chr8:38839821
|
T | C | 1 | a0001c0002t0002g0044 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1917-403T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839821 | ||||||
| chr8:38839881
|
T | A | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1917-343T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839881 | ||||||
| chr8:38839918
|
A | G | 1 | a0001c0001t0001g0022 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1917-306A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38839918 | ||||||
| chr8:38840059
|
T | TA | 88 | a0001c0001t0001g0022a0001c0001t0001g0200a0001c0001t0001g0213others(85): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1917-145dupA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 38840059 | |||||
| chr8:38840059
|
T | TAA | 7 | a0001c0001t0001g0106a0001c0001t0025g0118a0001c0003t0008g0090others(4): Show | 8 | HG02280.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1917-146_1917-145d others(4): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 38840059 | |||||
| chr8:38840085
|
C | T | 69 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(66): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1917-139C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38840085 | ||||||
| chr8:38840126
|
G | A | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1917-98G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38840126 | ||||||
| chr8:38840131
|
T | C | 174 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(171): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1917-93T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 8/12 | chr8 | 38840131 | ||||||
| chr8:38840510
|
C | A | 1 | a0001c0001t0023g0166 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1960+243C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38840510 | ||||||
| chr8:38840584
|
CA | C | 4 | a0001c0001t0007g0029a0001c0001t0007g0254a0001c0001t0007g0256others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1960+320delA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 38840584 | |||||
| chr8:38840867
|
T | C | 1 | a0001c0004t0011g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1960+600T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38840867 | ||||||
| chr8:38840937
|
T | C | 4 | a0001c0004t0020g0270a0001c0004t0020g0271a0001c0004t0020g0272others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1960+670T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38840937 | ||||||
| chr8:38841156
|
C | T | 1 | a0001c0002t0002g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1960+889C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38841156 | ||||||
| chr8:38841781
|
C | T | 16 | a0001c0002t0061g0242a0001c0003t0008g0002a0001c0003t0008g0084others(13): Show | 21 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1961-506C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38841781 | ||||||
| chr8:38841914
|
C | G | 1 | a0001c0003t0028g0092 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1961-373C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38841914 | ||||||
| chr8:38842003
|
G | A | 1 | a0001c0001t0005g0126 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1961-284G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38842003 | ||||||
| chr8:38842122
|
C | T | 1 | a0001c0001t0048g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1961-165C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38842122 | ||||||
| chr8:38842153
|
T | C | 1 | a0001c0001t0003g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1961-134T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38842153 | ||||||
| chr8:38842164
|
C | A | 1 | a0001c0001t0010g0111 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1961-123C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38842164 | ||||||
| chr8:38842193
|
C | T | 13 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(10): Show | 15 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1961-94C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38842193 | ||||||
| chr8:38842242
|
A | G | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1961-45A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 9/12 | chr8 | 38842242 | ||||||
| chr8:38842529
|
A | G | 4 | a0003c0007t0030g0228a0003c0007t0030g0231a0003c0007t0065g0229others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2121+82A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 10/12 | chr8 | 38842529 | ||||||
| chr8:38842964
|
C | T | 1 | a0001c0002t0002g0047 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2122-325C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 10/12 | chr8 | 38842964 | ||||||
| chr8:38843012
|
G | A | 1 | a0008c0017t0058g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2122-277G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 10/12 | chr8 | 38843012 | ||||||
| chr8:38843071
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0004g0159a0001c0001t0004g0197 | 3 | HG01168.hp1 NA19074.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2122-218C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 10/12 | chr8 | 38843071 | ||||||
| chr8:38843811
|
A | G | 172 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(169): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.2228+416A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38843811 | ||||||
| chr8:38843968
|
TTTATAA | T | 3 | a0001c0001t0007g0029a0001c0001t0007g0254a0001c0001t0063g0029 | 3 | HG02109.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2228+580_2228+585d others(8): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38843968 | |||||
| chr8:38844329
|
C | A | 1 | a0001c0002t0002g0038 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2228+934C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844329 | ||||||
| chr8:38844345
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2228+950T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844345 | ||||||
| chr8:38844359
|
A | G | 1 | a0004c0014t0070g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2228+964A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844359 | ||||||
| chr8:38844417
|
G | A | 1 | a0001c0001t0037g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2228+1022G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844417 | ||||||
| chr8:38844464
|
G | A | 1 | a0006c0016t0001g0190 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2228+1069G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844464 | ||||||
| chr8:38844465
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2228+1070C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844465 | ||||||
| chr8:38844476
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0212 | 2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2228+1081A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844476 | ||||||
| chr8:38844701
|
C | T | 1 | a0007c0012t0004g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2228+1306C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844701 | ||||||
| chr8:38844733
|
A | C | 1 | a0001c0006t0014g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2228+1338A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844733 | ||||||
| chr8:38844760
|
A | T | 60 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(57): Show | 68 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.2228+1365A>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844760 | ||||||
| chr8:38844828
|
T | A | 1 | a0001c0003t0008g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2228+1433T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844828 | ||||||
| chr8:38844952
|
TC | T | 3 | a0001c0001t0005g0027a0001c0001t0005g0232a0001c0001t0019g0027 | 3 | HG02155.hp2 HG04184.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2228+1558delC | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38844952 | ||||||
| chr8:38845000
|
C | T | 12 | a0001c0002t0006g0015a0001c0002t0006g0051a0001c0002t0006g0070others(9): Show | 13 | HG00408.hp1 HG02258.hp2 NA18956.hp2 others(10): Show |
intron_variant | MODIFIER | c.2228+1605C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38845000 | ||||||
| chr8:38845050
|
G | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.2229-1649G>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38845050 | ||||||
| chr8:38845093
|
T | G | 1 | a0001c0001t0003g0127 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2229-1606T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38845093 | ||||||
| chr8:38845125
|
A | G | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2229-1574A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38845125 | ||||||
| chr8:38845321
|
C | T | 5 | a0001c0001t0001g0155a0001c0001t0001g0168a0001c0001t0038g0163others(2): Show | 5 | HG02109.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2229-1378C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38845321 | ||||||
| chr8:38845422
|
C | T | 1 | a0001c0002t0006g0074 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2229-1277C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38845422 | ||||||
| chr8:38845679
|
T | G | 4 | a0001c0001t0007g0013a0001c0001t0007g0248a0001c0001t0007g0253others(1): Show | 6 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2229-1020T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38845679 | ||||||
| chr8:38845760
|
T | C | 7 | a0001c0001t0001g0236a0001c0001t0001g0239a0001c0001t0001g0240others(4): Show | 7 | HG00639.hp2 HG00642.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2229-939T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38845760 | ||||||
| chr8:38846279
|
A | G | 103 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0223others(100): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2229-420A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38846279 | ||||||
| chr8:38846283
|
C | CA | 32 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0145others(29): Show | 33 | HG00423.hp2 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.2229-389dupA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38846283 | |||||
| chr8:38846283
|
C | CAA | 52 | a0001c0002t0001g0223a0001c0002t0002g0004a0001c0002t0002g0005others(49): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.2229-390_2229-389d others(4): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38846283 | |||||
| chr8:38846283
|
C | CAAA | 21 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0224others(18): Show | 21 | HG00438.hp2 HG00735.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2229-391_2229-389d others(5): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38846283 | |||||
| chr8:38846283
|
CA | C | 11 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0176others(8): Show | 12 | HG02015.hp2 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2229-389delA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38846283 | |||||
| chr8:38846283
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0101a0001c0001t0001g0211a0001c0001t0003g0008others(2): Show | 5 | HG01109.hp2 HG03704.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.2229-398_2229-389d others(12): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38846283 | |||||
| chr8:38846283
|
CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0218others(4): Show | 7 | HG01975.hp1 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.2229-399_2229-389d others(13): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38846283 | |||||
| chr8:38846283
|
CAAAAAAA others(6): Show |
C | 10 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(7): Show | 12 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2229-401_2229-389d others(15): Show |
TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38846283 | |||||
| chr8:38846439
|
T | TA | 15 | a0001c0001t0004g0108a0001c0001t0007g0013a0001c0001t0007g0029others(12): Show | 18 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2229-244dupA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38846439 | |||||
| chr8:38846439
|
TA | T | 19 | a0001c0001t0001g0162a0001c0001t0004g0179a0001c0001t0018g0150others(16): Show | 24 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.2229-244delA | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 38846439 | |||||
| chr8:38846456
|
T | C | 1 | a0001c0002t0061g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2229-243T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38846456 | ||||||
| chr8:38846571
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2229-128T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38846571 | ||||||
| chr8:38846678
|
A | C | 23 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(20): Show | 26 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.2229-21A>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 11/12 | chr8 | 38846678 | ||||||
| chr8:38846856
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2349+37C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38846856 | ||||||
| chr8:38847108
|
T | G | 1 | a0001c0001t0005g0189 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2349+289T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847108 | ||||||
| chr8:38847247
|
T | G | 1 | a0003c0007t0030g0231 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2349+428T>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847247 | ||||||
| chr8:38847317
|
A | G | 8 | a0001c0004t0011g0014a0001c0004t0011g0276a0001c0004t0011g0277others(5): Show | 10 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2349+498A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847317 | ||||||
| chr8:38847441
|
A | G | 10 | a0001c0004t0013g0260a0001c0004t0013g0261a0001c0004t0013g0262others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2350-514A>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847441 | ||||||
| chr8:38847491
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2350-464T>C | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847491 | ||||||
| chr8:38847737
|
G | A | 2 | a0001c0004t0029g0274a0001c0004t0029g0275 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2350-218G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847737 | ||||||
| chr8:38847738
|
T | A | 2 | a0001c0004t0029g0274a0001c0004t0029g0275 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2350-217T>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847738 | ||||||
| chr8:38847739
|
C | A | 2 | a0001c0004t0029g0274a0001c0004t0029g0275 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2350-216C>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847739 | ||||||
| chr8:38847740
|
C | T | 2 | a0001c0004t0029g0274a0001c0004t0029g0275 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2350-215C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847740 | ||||||
| chr8:38847742
|
C | G | 2 | a0001c0004t0029g0274a0001c0004t0029g0275 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2350-213C>G | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847742 | ||||||
| chr8:38847876
|
G | A | 3 | a0001c0006t0014g0030a0001c0006t0014g0265a0001c0006t0014g0266 | 4 | HG02280.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2350-79G>A | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847876 | ||||||
| chr8:38847895
|
C | T | 1 | a0001c0002t0012g0050 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2350-60C>T | TACC1 | ENSG00000147526.20 | transcript | ENST00000317827.9 | protein_coding | 12/12 | chr8 | 38847895 |