Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7155 |
|---|---|
| ensemblid | ENSG00000077097.17 |
| hgncid | 11990 |
| symbol | TOP2B |
| name | DNA topoisomerase II beta |
| refseq_nuc | NM_001330700.2 |
| refseq_prot | NP_001317629.1 |
| ensembl_nuc | ENST00000264331.9 |
| ensembl_prot | ENSP00000264331.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 25597984 |
| end | 25664907 |
| strand | - |
| ver | v1.2 |
| region | chr3:25597984-25664907 |
| region5000 | chr3:25592984-25669907 |
| regionname0 | TOP2B_chr3_25597984_25664907 |
| regionname5000 | TOP2B_chr3_25592984_25669907 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1626 | 257 | 57 | 66 | 99 | 8 | 25 | 85 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0002 | 0/0 | 1626 | 31 | 0 | 0 | 28 | 0 | 3 | 23 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0003 | 0/0 | 1626 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0004 | 0/0 | 1626 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0005 | 0/0 | 1626 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0006 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0007 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0008 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0009 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0010 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0011 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4881 | 143 | 28 | 35 | 61 | 5 | 12 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0002 | 0/0 | 4881 | 94 | 12 | 30 | 37 | 3 | 12 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0003 | 0/0 | 4881 | 31 | 0 | 0 | 28 | 0 | 3 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0004 | 0/0 | 4881 | 10 | 10 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0005 | 0/0 | 4881 | 7 | 6 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0006 | 0/0 | 4881 | 6 | 4 | 2 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0007 | 0/0 | 4881 | 5 | 5 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0008 | 0/0 | 4881 | 3 | 0 | 3 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0009 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0010 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0011 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0012 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0013 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0014 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0015 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0016 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0017 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| c0018 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 934 | 145 | 25 | 37 | 63 | 5 | 13 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| t0002 | 0/0 | 934 | 140 | 38 | 29 | 56 | 2 | 15 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| t0003 | 0/0 | 937 | 11 | 0 | 0 | 11 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| t0004 | 0/0 | 934 | 4 | 1 | 2 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| t0005 | 0/0 | 934 | 3 | 0 | 3 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| t0006 | 0/0 | 928 | 3 | 3 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| t0007 | 0/0 | 937 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| t0008 | 0/0 | 934 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| t0009 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| t0010 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4881 | 143 | 28 | 35 | 61 | 5 | 12 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0002 | 0/0 | 4881 | 94 | 12 | 30 | 37 | 3 | 12 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0004 | 0/0 | 4881 | 10 | 10 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0007 | 0/0 | 4881 | 5 | 5 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0009 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0012 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0014 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0017 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0002c0003 | 0/0 | 4881 | 31 | 0 | 0 | 28 | 0 | 3 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0003c0005 | 0/0 | 4881 | 7 | 6 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0004c0006 | 0/0 | 4881 | 6 | 4 | 2 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0005c0008 | 0/0 | 4881 | 3 | 0 | 3 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0006c0010 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0007c0018 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0008c0013 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0009c0011 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0010c0015 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0011c0016 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5814 | 136 | 23 | 34 | 60 | 5 | 12 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0001t0002 | 0/0 | 5814 | 3 | 3 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0001t0003 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0001t0007 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0001t0008 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0001t0010 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0002t0001 | 0/0 | 5814 | 3 | 0 | 2 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0002t0002 | 0/0 | 5814 | 85 | 9 | 26 | 36 | 2 | 12 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0002t0004 | 0/0 | 5814 | 4 | 1 | 2 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0002t0006 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0002t0009 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0004t0002 | 0/0 | 5814 | 10 | 10 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0007t0002 | 0/0 | 5814 | 5 | 5 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0009t0006 | 0/0 | 5808 | 2 | 2 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0012t0001 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0014t0001 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0001c0017t0001 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0002c0003t0002 | 0/0 | 5814 | 22 | 0 | 0 | 19 | 0 | 3 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0002c0003t0003 | 0/0 | 5817 | 9 | 0 | 0 | 9 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0003c0005t0002 | 0/0 | 5814 | 7 | 6 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0004c0006t0002 | 0/0 | 5814 | 6 | 4 | 2 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0005c0008t0005 | 0/0 | 5814 | 3 | 0 | 3 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0006c0010t0003 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0007c0018t0001 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0008c0013t0001 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0009c0011t0001 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0010c0015t0002 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| a0011c0016t0002 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | copy fasta | chr3 | 25592984 | 25669907 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0008g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0001t0010g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0002t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0004t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0007t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0007t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0007t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0007t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0007t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0009t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0009t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0012t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0014t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0001c0017t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0002c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0003c0005t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0003c0005t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0003c0005t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0003c0005t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0003c0005t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0003c0005t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0003c0005t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0004c0006t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0004c0006t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0004c0006t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0004c0006t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0004c0006t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0004c0006t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0005c0008t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0005c0008t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0005c0008t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0006c0010t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0007c0018t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0008c0013t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0009c0011t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0010c0015t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| a0011c0016t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0066 | EUR | GBR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0033 | EUR | GBR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00408 | hp1 | a0002 | c0003 | t0002 | g0103 | EAS | CHS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | CHS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00621 | hp2 | a0002 | c0003 | t0002 | g0102 | EAS | CHS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0132 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00673 | hp1 | a0002 | c0003 | t0002 | g0130 | EAS | CHS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00741 | hp1 | a0001 | c0002 | t0004 | g0155 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0142 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0121 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0113 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0134 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01099 | hp1 | a0005 | c0008 | t0005 | g0157 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0095 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01175 | hp2 | a0005 | c0008 | t0005 | g0158 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01243 | hp2 | a0003 | c0005 | t0002 | g0043 | AMR | PUR | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01346 | hp1 | a0004 | c0006 | t0002 | g0090 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0122 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0070 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0143 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0154 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01884 | hp2 | a0001 | c0007 | t0002 | g0084 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01934 | hp2 | a0004 | c0006 | t0002 | g0086 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0072 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0110 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0138 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01993 | hp2 | a0001 | c0001 | t0008 | g0159 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02015 | hp2 | a0002 | c0003 | t0002 | g0126 | EAS | KHV | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | KHV | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02145 | hp1 | a0001 | c0009 | t0006 | g0293 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02145 | hp2 | a0001 | c0004 | t0002 | g0146 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0124 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CDX | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02155 | hp2 | a0002 | c0003 | t0002 | g0115 | EAS | CDX | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02280 | hp1 | a0001 | c0007 | t0002 | g0029 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02300 | hp2 | a0001 | c0012 | t0001 | g0238 | AMR | PEL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02572 | hp2 | a0001 | c0002 | t0006 | g0294 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02622 | hp1 | a0003 | c0005 | t0002 | g0082 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02717 | hp1 | a0008 | c0013 | t0001 | g0251 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0031 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02723 | hp2 | a0004 | c0006 | t0002 | g0089 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0112 | SAS | PJL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | PJL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02809 | hp1 | a0004 | c0006 | t0002 | g0093 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02809 | hp2 | a0001 | c0004 | t0002 | g0030 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02886 | hp1 | a0003 | c0005 | t0002 | g0049 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02886 | hp2 | a0001 | c0004 | t0002 | g0096 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02897 | hp2 | a0003 | c0005 | t0002 | g0048 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02922 | hp1 | a0007 | c0018 | t0001 | g0283 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02922 | hp2 | a0003 | c0005 | t0002 | g0044 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02976 | hp1 | a0001 | c0007 | t0002 | g0045 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0042 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03098 | hp2 | a0004 | c0006 | t0002 | g0094 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03130 | hp2 | a0001 | c0004 | t0002 | g0149 | AFR | ESN | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03209 | hp1 | a0001 | c0007 | t0002 | g0051 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03225 | hp1 | a0004 | c0006 | t0002 | g0088 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0297 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03540 | hp1 | a0001 | c0004 | t0002 | g0147 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | GWD | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03654 | hp1 | a0001 | c0017 | t0001 | g0285 | SAS | PJL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0136 | SAS | PJL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0127 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | BEB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03834 | hp1 | a0002 | c0003 | t0002 | g0105 | SAS | BEB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0025 | SAS | BEB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0119 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0135 | SAS | BEB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04184 | hp2 | a0002 | c0003 | t0002 | g0120 | SAS | BEB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0032 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | YRI | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18522 | hp2 | a0001 | c0009 | t0006 | g0295 | AFR | YRI | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18612 | hp2 | a0011 | c0016 | t0002 | g0101 | EAS | CHB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | CHB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | YRI | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18939 | hp2 | a0002 | c0003 | t0002 | g0116 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18942 | hp2 | a0002 | c0003 | t0003 | g0019 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18943 | hp2 | a0002 | c0003 | t0002 | g0123 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18944 | hp1 | a0002 | c0003 | t0003 | g0017 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18946 | hp2 | a0002 | c0003 | t0002 | g0117 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18950 | hp2 | a0002 | c0003 | t0002 | g0111 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18951 | hp1 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18952 | hp1 | a0002 | c0003 | t0002 | g0099 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18953 | hp1 | a0006 | c0010 | t0003 | g0013 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18960 | hp1 | a0002 | c0003 | t0002 | g0107 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18963 | hp2 | a0002 | c0003 | t0002 | g0109 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18964 | hp2 | a0002 | c0003 | t0003 | g0016 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18977 | hp1 | a0002 | c0003 | t0002 | g0108 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18982 | hp2 | a0002 | c0003 | t0003 | g0018 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18985 | hp1 | a0002 | c0003 | t0002 | g0118 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18989 | hp1 | a0001 | c0014 | t0001 | g0199 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18989 | hp2 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18993 | hp2 | a0002 | c0003 | t0003 | g0020 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19002 | hp2 | a0009 | c0011 | t0001 | g0220 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19011 | hp2 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19062 | hp1 | a0002 | c0003 | t0002 | g0129 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19081 | hp2 | a0002 | c0003 | t0002 | g0106 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19082 | hp1 | a0002 | c0003 | t0003 | g0021 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19084 | hp2 | a0002 | c0003 | t0002 | g0100 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19091 | hp2 | a0002 | c0003 | t0002 | g0104 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | YRI | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA20129 | hp1 | a0010 | c0015 | t0002 | g0087 | AFR | ASW | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0152 | AFR | ASW | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA20805 | hp1 | a0001 | c0002 | t0004 | g0153 | EUR | TSI | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | GIH | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0064 | SAS | GIH | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01123 | hp1 | a0005 | c0008 | t0005 | g0156 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0148 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02109 | hp2 | a0001 | c0002 | t0009 | g0296 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0150 | AFR | ACB | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03471 | hp1 | a0001 | c0007 | t0002 | g0050 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0144 | AFR | MSL | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | USA | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| HG06807 | hp2 | a0003 | c0005 | t0002 | g0092 | AFR | USA | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18955 | hp1 | a0002 | c0003 | t0002 | g0141 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | USA | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA20300 | hp2 | a0001 | c0004 | t0002 | g0145 | AFR | USA | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| NA21309 | hp2 | a0003 | c0005 | t0002 | g0091 | AFR | LWK | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0197 | REF | REF | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0165 | REF | REF | TOP2B_chr3_25592984_25669907 | TOP2B | chr3 | 25592984 | 25669907 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:25598337
|
T | A | 2 | a0005a0010 | 4 | HG01099.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
missense_variant | MODERATE | c.4851A>T | p.Glu1617Asp | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 36/36 | 5461/5814 | 4851/4881 | 1617/1626 | chr3 | 25598337 | ||
| chr3:25598386
|
C | G | 1 | a0009 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.4802G>C | p.Gly1601Ala | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 36/36 | 5412/5814 | 4802/4881 | 1601/1626 | chr3 | 25598386 | ||
| chr3:25599443
|
T | C | 2 | a0003a0008 | 8 | HG01243.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.4702A>G | p.Thr1568Ala | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/36 | 5312/5814 | 4702/4881 | 1568/1626 | chr3 | 25599443 | ||
| chr3:25604777
|
G | A | 3 | a0002a0006a0011 | 33 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(30): Show |
missense_variant | MODERATE | c.4472C>T | p.Thr1491Met | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/36 | 5082/5814 | 4472/4881 | 1491/1626 | chr3 | 25604777 | ||
| chr3:25609321
|
T | C | 2 | a0003a0004 | 13 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(10): Show |
missense_variant | MODERATE | c.3955A>G | p.Thr1319Ala | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/36 | 4565/5814 | 3955/4881 | 1319/1626 | chr3 | 25609321 | ||
| chr3:25637228
|
T | A | 1 | a0011 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.626A>T | p.His209Leu | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 6/36 | 1236/5814 | 626/4881 | 209/1626 | chr3 | 25637228 | ||
| chr3:25645304
|
G | A | 1 | a0007 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.236C>T | p.Thr79Met | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/36 | 846/5814 | 236/4881 | 79/1626 | chr3 | 25645304 | ||
| chr3:25664260
|
A | C | 1 | a0006 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.38T>G | p.Val13Gly | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 648/5814 | 38/4881 | 13/1626 | chr3 | 25664260 | ||
| chr3:25664267
|
C | T | 1 | a0005 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
missense_variant | MODERATE | c.31G>A | p.Ala11Thr | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 641/5814 | 31/4881 | 11/1626 | chr3 | 25664267 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:25598358
|
A | G | 1 | a0001c0012 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.4830T>C | p.Phe1610Phe | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 36/36 | 5440/5814 | 4830/4881 | 1610/1626 | chr3 | 25598358 | ||
| chr3:25612557
|
A | G | 1 | a0010c0015 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.3744T>C | p.Ala1248Ala | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/36 | 4354/5814 | 3744/4881 | 1248/1626 | chr3 | 25612557 | ||
| chr3:25615437
|
A | G | 1 | a0001c0007 | 5 | HG01884.hp2 HG02280.hp1 HG02976.hp1 others(2): Show |
synonymous_variant | LOW | c.3501T>C | p.Asp1167Asp | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 26/36 | 4111/5814 | 3501/4881 | 1167/1626 | chr3 | 25615437 | ||
| chr3:25623656
|
A | G | 1 | a0001c0009 | 2 | HG02145.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.2586T>C | p.Tyr862Tyr | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/36 | 3196/5814 | 2586/4881 | 862/1626 | chr3 | 25623656 | ||
| chr3:25624775
|
T | C | 1 | a0001c0004 | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
synonymous_variant | LOW | c.2253A>G | p.Leu751Leu | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 19/36 | 2863/5814 | 2253/4881 | 751/1626 | chr3 | 25624775 | ||
| chr3:25628947
|
G | A | 1 | a0001c0014 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.1806C>T | p.Ser602Ser | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/36 | 2416/5814 | 1806/4881 | 602/1626 | chr3 | 25628947 | ||
| chr3:25638247
|
T | C | 9 | a0001c0002a0001c0007a0001c0009others(6): Show | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
synonymous_variant | LOW | c.459A>G | p.Val153Val | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/36 | 1069/5814 | 459/4881 | 153/1626 | chr3 | 25638247 | ||
| chr3:25638262
|
T | C | 1 | a0001c0017 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.444A>G | p.Val148Val | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/36 | 1054/5814 | 444/4881 | 148/1626 | chr3 | 25638262 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:25598275
|
T | C | 1 | a0001c0002t0009 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*32A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 36/36 | 32 | chr3 | 25598275 | |||||
| chr3:25598283
|
A | G | 1 | a0001c0002t0009 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 36/36 | 24 | chr3 | 25598283 | |||||
| chr3:25664536
|
C | T | 2 | a0001c0002t0006a0001c0009t0006 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-239G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 239 | chr3 | 25664536 | |||||
| chr3:25664580
|
G | C | 1 | a0001c0002t0004 | 4 | HG00741.hp1 HG01433.hp1 NA20129.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-283C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 283 | chr3 | 25664580 | |||||
| chr3:25664639
|
C | A | 1 | a0005c0008t0005 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
5_prime_UTR_variant | MODIFIER | c.-342G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 342 | chr3 | 25664639 | |||||
| chr3:25664750
|
A | G | 1 | a0001c0001t0008 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-453T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 453 | chr3 | 25664750 | |||||
| chr3:25664786
|
A | C | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(15): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
5_prime_UTR_variant | MODIFIER | c.-489T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 489 | chr3 | 25664786 | |||||
| chr3:25664849
|
A | AGCC | 4 | a0001c0001t0003a0001c0001t0007a0002c0003t0003others(1): Show | 12 | HG01884.hp1 NA18942.hp2 NA18944.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-555_-553dupGGC | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 553 | chr3 | 25664849 | |||||
| chr3:25664849
|
AGCCGCC | A | 2 | a0001c0002t0006a0001c0009t0006 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-558_-553delGGCGGC | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 553 | chr3 | 25664849 | |||||
| chr3:25664856
|
G | A | 1 | a0001c0002t0009 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-559C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 559 | chr3 | 25664856 | |||||
| chr3:25664859
|
G | A | 1 | a0001c0001t0010 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-562C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/36 | 562 | chr3 | 25664859 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:25598482
|
A | AT | 159 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0250others(156): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
splice_region_variant&intron_variant | LOW | c.4711-6dupA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25598482 | ||||||
| chr3:25598579
|
A | C | 16 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295others(13): Show | 16 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.4711-102T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25598579 | ||||||
| chr3:25598614
|
T | C | 5 | a0001c0002t0002g0125a0001c0002t0002g0128a0001c0002t0002g0133others(2): Show | 5 | NA18747.hp2 NA18941.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.4711-137A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25598614 | ||||||
| chr3:25598748
|
A | G | 1 | a0001c0002t0002g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4711-271T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25598748 | ||||||
| chr3:25598867
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4711-390C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25598867 | ||||||
| chr3:25598928
|
G | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4711-451C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25598928 | ||||||
| chr3:25598974
|
C | G | 81 | a0001c0001t0001g0172a0001c0002t0001g0288a0001c0002t0002g0001others(78): Show | 88 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.4710+461G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25598974 | ||||||
| chr3:25599007
|
A | AAAT | 3 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0082 | 3 | HG01243.hp2 HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4710+425_4710+427d others(5): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25599007 | ||||||
| chr3:25599031
|
T | C | 2 | a0001c0001t0001g0249a0001c0012t0001g0238 | 2 | HG01243.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4710+404A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25599031 | ||||||
| chr3:25599200
|
C | G | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4710+235G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25599200 | ||||||
| chr3:25599256
|
A | G | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4710+179T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25599256 | ||||||
| chr3:25599323
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.4710+112G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25599323 | ||||||
| chr3:25599324
|
G | A | 13 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.4710+111C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25599324 | ||||||
| chr3:25599329
|
G | A | 1 | a0001c0002t0002g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4710+106C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 35/35 | chr3 | 25599329 | ||||||
| chr3:25599597
|
A | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.4616-68T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25599597 | ||||||
| chr3:25599798
|
T | C | 1 | a0002c0003t0002g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4616-269A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25599798 | ||||||
| chr3:25599866
|
T | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4616-337A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25599866 | ||||||
| chr3:25600293
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4616-764G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600293 | ||||||
| chr3:25600349
|
G | C | 70 | a0001c0001t0001g0172a0001c0001t0001g0284a0001c0001t0002g0151others(67): Show | 77 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.4615+751C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600349 | ||||||
| chr3:25600533
|
T | C | 61 | a0001c0001t0001g0173a0001c0001t0001g0222a0001c0002t0002g0110others(58): Show | 61 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4615+567A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600533 | ||||||
| chr3:25600576
|
AT | A | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4615+523delA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600576 | ||||||
| chr3:25600614
|
A | C | 65 | a0001c0001t0001g0172a0001c0001t0002g0151a0001c0001t0010g0297others(62): Show | 72 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.4615+486T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600614 | ||||||
| chr3:25600627
|
A | G | 14 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(11): Show | 14 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.4615+473T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600627 | ||||||
| chr3:25600666
|
T | C | 94 | a0001c0001t0001g0172a0001c0001t0001g0284a0001c0001t0002g0151others(91): Show | 101 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.4615+434A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600666 | ||||||
| chr3:25600729
|
G | A | 1 | a0001c0007t0002g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4615+371C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600729 | ||||||
| chr3:25600811
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4615+289G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600811 | ||||||
| chr3:25600945
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0197 | 3 | HG00099.hp1 HG02451.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4615+155A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 34/35 | chr3 | 25600945 | ||||||
| chr3:25601268
|
AC | A | 13 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.4490-44delG | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25601268 | ||||||
| chr3:25601316
|
G | A | 2 | a0001c0002t0002g0076a0001c0002t0002g0080 | 2 | NA18994.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.4490-91C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25601316 | ||||||
| chr3:25601388
|
C | T | 1 | a0002c0003t0003g0021 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.4490-163G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25601388 | ||||||
| chr3:25601442
|
A | C | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4490-217T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25601442 | ||||||
| chr3:25601569
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4490-344G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25601569 | ||||||
| chr3:25602012
|
A | T | 6 | a0004c0006t0002g0086a0004c0006t0002g0088a0004c0006t0002g0089others(3): Show | 6 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4490-787T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602012 | ||||||
| chr3:25602024
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4490-799A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602024 | ||||||
| chr3:25602139
|
T | C | 1 | a0001c0002t0002g0125 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.4490-914A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602139 | ||||||
| chr3:25602193
|
C | T | 1 | a0001c0004t0002g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4490-968G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602193 | ||||||
| chr3:25602406
|
AAAAG | A | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4490-1185_4490-118 others(8): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602406 | ||||||
| chr3:25602410
|
G | A | 138 | a0001c0001t0001g0172a0001c0002t0001g0288a0001c0002t0002g0001others(135): Show | 145 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.4490-1185C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602410 | ||||||
| chr3:25602415
|
A | AAAG | 13 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.4490-1191_4490-119 others(7): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602415 | ||||||
| chr3:25602415
|
A | G | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4490-1190T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602415 | ||||||
| chr3:25602416
|
G | A | 149 | a0001c0001t0001g0172a0001c0002t0001g0288a0001c0002t0002g0001others(146): Show | 156 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.4490-1191C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602416 | ||||||
| chr3:25602416
|
G | GA | 56 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0161others(53): Show | 58 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.4490-1192dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602416 | ||||||
| chr3:25602417
|
A | AAG | 11 | a0001c0002t0002g0042a0001c0002t0002g0053a0001c0002t0002g0057others(8): Show | 11 | HG00423.hp2 HG01192.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.4490-1193_4490-119 others(6): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602417 | ||||||
| chr3:25602417
|
A | AG | 54 | a0001c0001t0001g0172a0001c0002t0001g0288a0001c0002t0002g0001others(51): Show | 61 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.4490-1193_4490-119 others(5): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602417 | ||||||
| chr3:25602417
|
A | G | 1 | a0001c0002t0002g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4490-1192T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602417 | ||||||
| chr3:25602418
|
A | G | 57 | a0001c0002t0002g0034a0001c0002t0002g0110a0001c0002t0002g0112others(54): Show | 57 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.4490-1193T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602418 | ||||||
| chr3:25602468
|
G | A | 1 | a0001c0002t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4490-1243C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602468 | ||||||
| chr3:25602498
|
TA | T | 152 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0276others(149): Show | 159 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.4490-1274delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602498 | ||||||
| chr3:25602553
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.4490-1328A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602553 | ||||||
| chr3:25602687
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.4490-1462A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602687 | ||||||
| chr3:25602724
|
C | G | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4490-1499G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602724 | ||||||
| chr3:25602900
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4490-1675A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25602900 | ||||||
| chr3:25603341
|
C | T | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.4489+1419G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603341 | ||||||
| chr3:25603389
|
T | C | 151 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(148): Show | 158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.4489+1371A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603389 | ||||||
| chr3:25603408
|
A | G | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4489+1352T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603408 | ||||||
| chr3:25603446
|
T | C | 16 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0166others(13): Show | 16 | HG00621.hp1 HG01255.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.4489+1314A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603446 | ||||||
| chr3:25603458
|
G | T | 5 | a0001c0002t0002g0125a0001c0002t0002g0128a0001c0002t0002g0133others(2): Show | 5 | NA18747.hp2 NA18941.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.4489+1302C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603458 | ||||||
| chr3:25603481
|
A | G | 154 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(151): Show | 161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.4489+1279T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603481 | ||||||
| chr3:25603535
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4489+1225C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603535 | ||||||
| chr3:25603630
|
T | A | 153 | a0001c0001t0001g0172a0001c0002t0001g0288a0001c0002t0002g0001others(150): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.4489+1130A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603630 | ||||||
| chr3:25603772
|
C | G | 156 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0151others(153): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.4489+988G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603772 | ||||||
| chr3:25603885
|
G | A | 1 | a0001c0002t0002g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4489+875C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603885 | ||||||
| chr3:25603930
|
C | A | 150 | a0001c0001t0001g0172a0001c0002t0001g0288a0001c0002t0002g0001others(147): Show | 157 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.4489+830G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25603930 | ||||||
| chr3:25604023
|
G | A | 157 | a0001c0001t0001g0172a0001c0001t0002g0097a0001c0001t0002g0098others(154): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.4489+737C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25604023 | ||||||
| chr3:25604073
|
T | C | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4489+687A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25604073 | ||||||
| chr3:25604078
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4489+682C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25604078 | ||||||
| chr3:25604158
|
T | A | 1 | a0001c0002t0002g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4489+602A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25604158 | ||||||
| chr3:25604206
|
G | GT | 14 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(11): Show | 14 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.4489+553_4489+554i others(3): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25604206 | ||||||
| chr3:25604207
|
G | T | 150 | a0001c0001t0001g0172a0001c0002t0001g0288a0001c0002t0002g0001others(147): Show | 157 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.4489+553C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25604207 | ||||||
| chr3:25604540
|
C | T | 62 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(59): Show | 69 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.4489+220G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 33/35 | chr3 | 25604540 | ||||||
| chr3:25605497
|
C | T | 1 | a0001c0002t0002g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4378+546G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 32/35 | chr3 | 25605497 | ||||||
| chr3:25605508
|
TA | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4378+534delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 32/35 | chr3 | 25605508 | ||||||
| chr3:25605567
|
T | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4378+476A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 32/35 | chr3 | 25605567 | ||||||
| chr3:25605693
|
A | C | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4378+350T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 32/35 | chr3 | 25605693 | ||||||
| chr3:25605917
|
A | G | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4378+126T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 32/35 | chr3 | 25605917 | ||||||
| chr3:25606141
|
A | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0174a0001c0001t0001g0179others(7): Show | 11 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.4299-19T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 31/35 | chr3 | 25606141 | ||||||
| chr3:25606144
|
C | A | 1 | a0001c0001t0001g0279 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4299-22G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 31/35 | chr3 | 25606144 | ||||||
| chr3:25607099
|
A | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.4298+72T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 31/35 | chr3 | 25607099 | ||||||
| chr3:25607582
|
G | A | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4094-207C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25607582 | ||||||
| chr3:25607612
|
A | G | 62 | a0001c0001t0001g0173a0001c0002t0002g0034a0001c0002t0002g0110others(59): Show | 62 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.4094-237T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25607612 | ||||||
| chr3:25607853
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG00738.hp2 HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.4094-478G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25607853 | ||||||
| chr3:25607896
|
C | T | 4 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295others(1): Show | 4 | HG02145.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.4094-521G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25607896 | ||||||
| chr3:25608029
|
CCCT | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4094-657_4094-655d others(5): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608029 | ||||||
| chr3:25608074
|
T | A | 154 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(151): Show | 161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.4094-699A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608074 | ||||||
| chr3:25608207
|
C | T | 1 | a0001c0002t0002g0127 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4094-832G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608207 | ||||||
| chr3:25608270
|
A | C | 8 | a0001c0001t0001g0161a0001c0001t0001g0171a0001c0001t0001g0177others(5): Show | 8 | HG02897.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.4094-895T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608270 | ||||||
| chr3:25608424
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4093+759A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608424 | ||||||
| chr3:25608705
|
T | C | 1 | a0001c0002t0009g0296 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4093+478A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608705 | ||||||
| chr3:25608796
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4093+387A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608796 | ||||||
| chr3:25608816
|
G | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4093+367C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608816 | ||||||
| chr3:25608872
|
C | T | 1 | a0001c0001t0007g0024 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4093+311G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608872 | ||||||
| chr3:25608902
|
G | C | 1 | a0001c0002t0002g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4093+281C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25608902 | ||||||
| chr3:25609037
|
T | C | 151 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(148): Show | 158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.4093+146A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25609037 | ||||||
| chr3:25609038
|
G | A | 2 | a0002c0003t0002g0105a0002c0003t0002g0120 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4093+145C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 30/35 | chr3 | 25609038 | ||||||
| chr3:25609387
|
A | G | 1 | a0001c0002t0004g0153 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3932-43T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 29/35 | chr3 | 25609387 | ||||||
| chr3:25609432
|
T | C | 4 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295others(1): Show | 4 | HG02145.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3932-88A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 29/35 | chr3 | 25609432 | ||||||
| chr3:25610022
|
CT | C | 12 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.3787-311delA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25610022 | ||||||
| chr3:25610183
|
C | CA | 11 | a0001c0002t0002g0062a0001c0004t0002g0030a0001c0004t0002g0031others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3787-472dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25610183 | ||||||
| chr3:25610183
|
CA | C | 7 | a0001c0001t0001g0167a0001c0001t0001g0256a0001c0001t0001g0268others(4): Show | 7 | HG01358.hp1 HG02015.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3787-472delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25610183 | ||||||
| chr3:25610413
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3787-701A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25610413 | ||||||
| chr3:25610549
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3787-837A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25610549 | ||||||
| chr3:25610558
|
A | G | 1 | a0001c0007t0002g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3787-846T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25610558 | ||||||
| chr3:25610620
|
A | G | 155 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0151others(152): Show | 162 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.3787-908T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25610620 | ||||||
| chr3:25611012
|
T | G | 151 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(148): Show | 158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.3787-1300A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25611012 | ||||||
| chr3:25611299
|
G | C | 1 | a0001c0002t0002g0075 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3786+1216C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25611299 | ||||||
| chr3:25611299
|
G | T | 1 | a0001c0001t0001g0246 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3786+1216C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25611299 | ||||||
| chr3:25611319
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3786+1196C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25611319 | ||||||
| chr3:25611929
|
G | C | 1 | a0001c0001t0001g0190 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3786+586C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25611929 | ||||||
| chr3:25612133
|
G | C | 1 | a0001c0002t0002g0066 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3786+382C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25612133 | ||||||
| chr3:25612504
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3786+11C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25612504 | ||||||
| chr3:25612507
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
splice_region_variant&intron_variant | LOW | c.3786+8A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 28/35 | chr3 | 25612507 | ||||||
| chr3:25612873
|
T | A | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3592-164A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25612873 | ||||||
| chr3:25612990
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3592-281C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25612990 | ||||||
| chr3:25613160
|
T | A | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3592-451A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25613160 | ||||||
| chr3:25613186
|
A | G | 79 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0161others(76): Show | 81 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.3592-477T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25613186 | ||||||
| chr3:25613299
|
C | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3592-590G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25613299 | ||||||
| chr3:25613344
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3592-635A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25613344 | ||||||
| chr3:25613600
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3592-891C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25613600 | ||||||
| chr3:25613727
|
C | CA | 15 | a0001c0001t0001g0185a0001c0001t0001g0224a0001c0001t0001g0258others(12): Show | 15 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3592-1019dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25613727 | ||||||
| chr3:25613826
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3592-1117A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25613826 | ||||||
| chr3:25613842
|
T | C | 2 | a0005c0008t0005g0156a0005c0008t0005g0158 | 2 | HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3592-1133A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25613842 | ||||||
| chr3:25613886
|
C | G | 122 | a0001c0001t0001g0173a0001c0002t0001g0288a0001c0002t0002g0001others(119): Show | 129 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.3592-1177G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25613886 | ||||||
| chr3:25614234
|
G | C | 1 | a0001c0001t0001g0008 | 2 | NA18986.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3591+971C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614234 | ||||||
| chr3:25614290
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3591+915T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614290 | ||||||
| chr3:25614301
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3591+904A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614301 | ||||||
| chr3:25614302
|
CAAT | C | 59 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(56): Show | 66 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.3591+900_3591+902d others(5): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614302 | ||||||
| chr3:25614339
|
T | C | 60 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(57): Show | 67 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.3591+866A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614339 | ||||||
| chr3:25614504
|
A | C | 60 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(57): Show | 67 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.3591+701T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614504 | ||||||
| chr3:25614521
|
G | C | 1 | a0003c0005t0002g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3591+684C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614521 | ||||||
| chr3:25614541
|
T | A | 3 | a0002c0003t0002g0100a0002c0003t0002g0116a0002c0003t0002g0117 | 3 | NA18939.hp2 NA18946.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3591+664A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614541 | ||||||
| chr3:25614595
|
T | C | 1 | a0004c0006t0002g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3591+610A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614595 | ||||||
| chr3:25614694
|
C | T | 2 | a0001c0002t0002g0046a0001c0002t0002g0047 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3591+511G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614694 | ||||||
| chr3:25614711
|
A | G | 1 | a0003c0005t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3591+494T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614711 | ||||||
| chr3:25614966
|
A | T | 138 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(135): Show | 145 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3591+239T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25614966 | ||||||
| chr3:25615100
|
T | G | 1 | a0001c0001t0001g0281 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3591+105A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 27/35 | chr3 | 25615100 | ||||||
| chr3:25615654
|
ATAAT | A | 13 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.3352-72_3352-69del others(4): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25615654 | ||||||
| chr3:25615688
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3352-102A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25615688 | ||||||
| chr3:25615832
|
C | A | 62 | a0001c0001t0001g0173a0001c0002t0002g0034a0001c0002t0002g0110others(59): Show | 62 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.3352-246G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25615832 | ||||||
| chr3:25616125
|
T | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0214a0001c0001t0001g0241 | 4 | NA18612.hp1 NA19054.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.3352-539A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25616125 | ||||||
| chr3:25616413
|
G | GA | 143 | a0001c0001t0001g0173a0001c0001t0001g0227a0001c0001t0001g0247others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.3352-828dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25616413 | ||||||
| chr3:25616484
|
C | G | 8 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(5): Show | 8 | HG01243.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.3352-898G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25616484 | ||||||
| chr3:25616750
|
T | G | 1 | a0001c0001t0001g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3352-1164A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25616750 | ||||||
| chr3:25616995
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3352-1409T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25616995 | ||||||
| chr3:25617126
|
A | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3351+1292T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25617126 | ||||||
| chr3:25617152
|
T | C | 1 | a0001c0002t0006g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3351+1266A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25617152 | ||||||
| chr3:25617225
|
A | T | 67 | a0001c0001t0001g0225a0001c0001t0001g0234a0001c0002t0002g0034others(64): Show | 67 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.3351+1193T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25617225 | ||||||
| chr3:25617292
|
T | C | 1 | a0001c0007t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3351+1126A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25617292 | ||||||
| chr3:25617930
|
G | C | 1 | a0001c0002t0002g0028 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3351+488C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25617930 | ||||||
| chr3:25618029
|
G | A | 1 | a0003c0005t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3351+389C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25618029 | ||||||
| chr3:25618131
|
T | G | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3351+287A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25618131 | ||||||
| chr3:25618189
|
T | C | 4 | a0001c0001t0001g0172a0001c0002t0002g0003a0001c0002t0002g0063others(1): Show | 5 | NA18944.hp2 NA18970.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.3351+229A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 25/35 | chr3 | 25618189 | ||||||
| chr3:25618603
|
G | GT | 144 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(141): Show | 151 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.3259+50dupA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 24/35 | chr3 | 25618603 | ||||||
| chr3:25618603
|
G | GTT | 7 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(4): Show | 7 | HG01243.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3259+49_3259+50dup others(2): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 24/35 | chr3 | 25618603 | ||||||
| chr3:25618631
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3259+23T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 24/35 | chr3 | 25618631 | ||||||
| chr3:25618856
|
A | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
splice_region_variant&intron_variant | LOW | c.3064-7T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25618856 | ||||||
| chr3:25619161
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3064-312A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619161 | ||||||
| chr3:25619184
|
T | C | 151 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(148): Show | 158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.3064-335A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619184 | ||||||
| chr3:25619208
|
G | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0166a0001c0001t0001g0206others(3): Show | 6 | HG00621.hp1 NA18956.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.3064-359C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619208 | ||||||
| chr3:25619211
|
C | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3064-362G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619211 | ||||||
| chr3:25619244
|
C | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-395G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619244 | ||||||
| chr3:25619284
|
C | A | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-435G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619284 | ||||||
| chr3:25619285
|
T | A | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-436A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619285 | ||||||
| chr3:25619287
|
T | G | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-438A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619287 | ||||||
| chr3:25619288
|
A | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-439T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619288 | ||||||
| chr3:25619293
|
A | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-444T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619293 | ||||||
| chr3:25619294
|
G | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-445C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619294 | ||||||
| chr3:25619296
|
C | CT | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-448_3064-447i others(3): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619296 | ||||||
| chr3:25619297
|
A | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-448T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619297 | ||||||
| chr3:25619298
|
C | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-449G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619298 | ||||||
| chr3:25619301
|
A | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-452T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619301 | ||||||
| chr3:25619302
|
A | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-453T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619302 | ||||||
| chr3:25619303
|
ACT | A | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3064-456_3064-455d others(4): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619303 | ||||||
| chr3:25619601
|
A | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3063+261T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619601 | ||||||
| chr3:25619646
|
G | A | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3063+216C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619646 | ||||||
| chr3:25619710
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3063+152A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619710 | ||||||
| chr3:25619738
|
G | GA | 16 | a0001c0001t0001g0190a0001c0001t0001g0207a0001c0001t0001g0232others(13): Show | 16 | HG00741.hp2 HG01099.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3063+123dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619738 | ||||||
| chr3:25619738
|
GA | G | 24 | a0001c0001t0001g0177a0001c0001t0001g0205a0001c0001t0001g0212others(21): Show | 24 | HG01167.hp2 HG01346.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.3063+123delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 23/35 | chr3 | 25619738 | ||||||
| chr3:25620066
|
T | TA | 151 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(148): Show | 158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
splice_region_variant&intron_variant | LOW | c.2863-5dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620066 | ||||||
| chr3:25620231
|
C | T | 1 | a0009c0011t0001g0220 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2863-169G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620231 | ||||||
| chr3:25620256
|
T | C | 1 | a0001c0002t0002g0054 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2863-194A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620256 | ||||||
| chr3:25620368
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2863-306C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620368 | ||||||
| chr3:25620470
|
A | T | 1 | a0008c0013t0001g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2862+212T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620470 | ||||||
| chr3:25620495
|
C | G | 1 | a0001c0001t0001g0271 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2862+187G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620495 | ||||||
| chr3:25620605
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2862+77G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620605 | ||||||
| chr3:25620645
|
T | G | 1 | a0001c0001t0001g0008 | 2 | NA18986.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2862+37A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620645 | ||||||
| chr3:25620647
|
C | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2862+35G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620647 | ||||||
| chr3:25620668
|
A | G | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2862+14T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 22/35 | chr3 | 25620668 | ||||||
| chr3:25620861
|
C | T | 1 | a0001c0002t0002g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2728-45G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25620861 | ||||||
| chr3:25620864
|
T | C | 1 | a0001c0002t0002g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2728-48A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25620864 | ||||||
| chr3:25621055
|
G | A | 1 | a0001c0001t0001g0008 | 2 | NA18986.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2728-239C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25621055 | ||||||
| chr3:25621143
|
C | G | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2728-327G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25621143 | ||||||
| chr3:25621661
|
C | T | 159 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0097others(156): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.2728-845G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25621661 | ||||||
| chr3:25621747
|
G | C | 60 | a0001c0001t0001g0173a0001c0002t0002g0110a0001c0002t0002g0112others(57): Show | 60 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.2728-931C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25621747 | ||||||
| chr3:25621755
|
A | G | 152 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(149): Show | 159 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2728-939T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25621755 | ||||||
| chr3:25621787
|
G | C | 129 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(126): Show | 136 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.2728-971C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25621787 | ||||||
| chr3:25621893
|
A | G | 210 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0161others(207): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.2728-1077T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25621893 | ||||||
| chr3:25621916
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2728-1100C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25621916 | ||||||
| chr3:25622422
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2727+1093A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622422 | ||||||
| chr3:25622479
|
C | T | 157 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0151others(154): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2727+1036G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622479 | ||||||
| chr3:25622547
|
A | G | 3 | a0002c0003t0002g0102a0002c0003t0002g0104a0002c0003t0002g0141 | 3 | HG00621.hp2 NA18955.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2727+968T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622547 | ||||||
| chr3:25622623
|
TA | T | 5 | a0001c0007t0002g0050a0001c0007t0002g0051a0001c0007t0002g0084others(2): Show | 5 | HG01884.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2727+891delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622623 | ||||||
| chr3:25622639
|
A | AT | 28 | a0001c0001t0001g0171a0001c0001t0001g0176a0001c0001t0001g0180others(25): Show | 30 | HG01106.hp2 HG01109.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.2727+875dupA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622639 | ||||||
| chr3:25622701
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2727+814G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622701 | ||||||
| chr3:25622725
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2727+790G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622725 | ||||||
| chr3:25622741
|
A | G | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2727+774T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622741 | ||||||
| chr3:25622873
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2727+642G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622873 | ||||||
| chr3:25622920
|
C | A | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2727+595G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622920 | ||||||
| chr3:25622964
|
G | C | 1 | a0001c0001t0001g0008 | 2 | NA18986.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2727+551C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622964 | ||||||
| chr3:25622966
|
T | C | 159 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0097others(156): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.2727+549A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25622966 | ||||||
| chr3:25623097
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2727+418A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25623097 | ||||||
| chr3:25623152
|
T | A | 129 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(126): Show | 136 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.2727+363A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25623152 | ||||||
| chr3:25623207
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2727+308C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25623207 | ||||||
| chr3:25623339
|
C | T | 14 | a0001c0001t0001g0173a0001c0002t0002g0110a0001c0002t0002g0112others(11): Show | 14 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2727+176G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25623339 | ||||||
| chr3:25623402
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2727+113G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 21/35 | chr3 | 25623402 | ||||||
| chr3:25623841
|
T | C | 1 | a0001c0002t0002g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2496-95A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 20/35 | chr3 | 25623841 | ||||||
| chr3:25624068
|
T | C | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2495+229A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 20/35 | chr3 | 25624068 | ||||||
| chr3:25624665
|
C | T | 59 | a0001c0002t0002g0110a0001c0002t0002g0112a0001c0002t0002g0113others(56): Show | 59 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.2346+17G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 19/35 | chr3 | 25624665 | ||||||
| chr3:25624994
|
G | A | 62 | a0001c0001t0001g0172a0001c0002t0001g0288a0001c0002t0002g0001others(59): Show | 69 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.2225-191C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25624994 | ||||||
| chr3:25625079
|
A | G | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2225-276T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625079 | ||||||
| chr3:25625091
|
T | C | 155 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(152): Show | 162 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.2225-288A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625091 | ||||||
| chr3:25625211
|
G | A | 152 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(149): Show | 159 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2225-408C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625211 | ||||||
| chr3:25625532
|
T | TTTTG | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2225-733_2225-730d others(6): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625532 | ||||||
| chr3:25625532
|
T | TTTTGTTT others(1): Show |
152 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(149): Show | 159 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2225-737_2225-730d others(10): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625532 | ||||||
| chr3:25625570
|
G | GT | 5 | a0001c0001t0001g0163a0001c0001t0001g0225a0001c0002t0002g0035others(2): Show | 5 | HG00639.hp2 HG01192.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2225-768dupA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625570 | ||||||
| chr3:25625570
|
G | T | 2 | a0001c0001t0001g0170a0001c0002t0002g0068 | 2 | HG02004.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2225-767C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625570 | ||||||
| chr3:25625707
|
G | C | 1 | a0001c0002t0002g0143 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2224+853C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625707 | ||||||
| chr3:25625733
|
A | C | 3 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037 | 3 | HG00639.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2224+827T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625733 | ||||||
| chr3:25625773
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2224+787A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625773 | ||||||
| chr3:25625901
|
G | T | 3 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037 | 3 | HG00639.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2224+659C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625901 | ||||||
| chr3:25625902
|
A | T | 3 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037 | 3 | HG00639.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2224+658T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25625902 | ||||||
| chr3:25626258
|
T | A | 2 | a0002c0003t0002g0100a0002c0003t0002g0116 | 2 | NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2224+302A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25626258 | ||||||
| chr3:25626439
|
G | A | 13 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.2224+121C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25626439 | ||||||
| chr3:25626517
|
T | C | 1 | a0001c0002t0006g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2224+43A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 18/35 | chr3 | 25626517 | ||||||
| chr3:25626933
|
A | G | 10 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(7): Show | 13 | NA18951.hp2 NA18980.hp1 NA18983.hp2 others(10): Show |
intron_variant | MODIFIER | c.2017-69T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 16/35 | chr3 | 25626933 | ||||||
| chr3:25626986
|
T | A | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2017-122A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 16/35 | chr3 | 25626986 | ||||||
| chr3:25627054
|
T | C | 1 | a0002c0003t0002g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2016+133A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 16/35 | chr3 | 25627054 | ||||||
| chr3:25627414
|
A | AGTGATCA others(311): Show |
3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1907-119_1907-118i others(320): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25627414 | ||||||
| chr3:25627735
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0179 | 3 | HG01081.hp1 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1907-439G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25627735 | ||||||
| chr3:25627844
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1907-548G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25627844 | ||||||
| chr3:25627859
|
C | T | 1 | a0001c0002t0002g0035 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1907-563G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25627859 | ||||||
| chr3:25627948
|
C | A | 1 | a0001c0002t0002g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1907-652G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25627948 | ||||||
| chr3:25627960
|
C | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1907-664G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25627960 | ||||||
| chr3:25628000
|
C | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1907-704G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628000 | ||||||
| chr3:25628001
|
G | A | 1 | a0001c0002t0002g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1907-705C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628001 | ||||||
| chr3:25628069
|
T | TA | 123 | a0001c0001t0001g0291a0001c0002t0001g0288a0001c0002t0002g0001others(120): Show | 130 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1907-774dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628069 | ||||||
| chr3:25628077
|
A | G | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1906+770T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628077 | ||||||
| chr3:25628080
|
G | A | 3 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037 | 3 | HG00639.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1906+767C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628080 | ||||||
| chr3:25628118
|
A | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1906+729T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628118 | ||||||
| chr3:25628166
|
T | G | 3 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0146 | 3 | HG02145.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1906+681A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628166 | ||||||
| chr3:25628171
|
T | TA | 128 | a0001c0001t0001g0011a0001c0001t0001g0272a0001c0001t0001g0273others(125): Show | 136 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1906+675dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628171 | ||||||
| chr3:25628171
|
TA | T | 13 | a0001c0001t0001g0237a0001c0001t0001g0278a0001c0004t0002g0030others(10): Show | 13 | HG01069.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1906+675delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628171 | ||||||
| chr3:25628368
|
GC | G | 139 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(136): Show | 146 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1906+478delG | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628368 | ||||||
| chr3:25628369
|
C | G | 66 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0161others(63): Show | 68 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1906+478G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628369 | ||||||
| chr3:25628675
|
A | G | 149 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(146): Show | 156 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1906+172T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628675 | ||||||
| chr3:25628698
|
G | C | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1906+149C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628698 | ||||||
| chr3:25628786
|
T | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1906+61A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628786 | ||||||
| chr3:25628810
|
A | G | 5 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906+37T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 15/35 | chr3 | 25628810 | ||||||
| chr3:25629178
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1690-33A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 13/35 | chr3 | 25629178 | ||||||
| chr3:25629296
|
T | G | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1690-151A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 13/35 | chr3 | 25629296 | ||||||
| chr3:25629321
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0272a0001c0001t0001g0273others(1): Show | 5 | HG01255.hp2 HG01934.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1690-176A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 13/35 | chr3 | 25629321 | ||||||
| chr3:25629757
|
CTTG | C | 12 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1689+269_1689+271d others(5): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 13/35 | chr3 | 25629757 | ||||||
| chr3:25629796
|
C | T | 3 | a0001c0004t0002g0096a0001c0004t0002g0145a0001c0004t0002g0149 | 3 | HG02886.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1689+233G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 13/35 | chr3 | 25629796 | ||||||
| chr3:25629838
|
C | T | 1 | a0001c0001t0001g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1689+191G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 13/35 | chr3 | 25629838 | ||||||
| chr3:25630287
|
C | T | 140 | a0001c0001t0001g0173a0001c0002t0001g0288a0001c0002t0002g0001others(137): Show | 147 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1563+25G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 12/35 | chr3 | 25630287 | ||||||
| chr3:25630297
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1563+15G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 12/35 | chr3 | 25630297 | ||||||
| chr3:25631107
|
A | G | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1267-168T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25631107 | ||||||
| chr3:25631287
|
C | T | 154 | a0001c0001t0002g0151a0001c0001t0010g0297a0001c0002t0001g0288others(151): Show | 161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1267-348G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25631287 | ||||||
| chr3:25631542
|
A | G | 1 | a0001c0009t0006g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1267-603T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25631542 | ||||||
| chr3:25631553
|
T | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1267-614A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25631553 | ||||||
| chr3:25631577
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1267-638T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25631577 | ||||||
| chr3:25631589
|
C | T | 152 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(149): Show | 159 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1267-650G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25631589 | ||||||
| chr3:25631748
|
T | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | NA18953.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1266+698A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25631748 | ||||||
| chr3:25631996
|
G | A | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1266+450C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25631996 | ||||||
| chr3:25632200
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1266+246T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25632200 | ||||||
| chr3:25632266
|
T | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0172others(22): Show | 27 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1266+180A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25632266 | ||||||
| chr3:25632285
|
C | T | 125 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(122): Show | 132 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1266+161G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25632285 | ||||||
| chr3:25632344
|
A | C | 123 | a0001c0001t0001g0173a0001c0002t0001g0288a0001c0002t0002g0001others(120): Show | 130 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1266+102T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25632344 | ||||||
| chr3:25632397
|
C | G | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1266+49G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 10/35 | chr3 | 25632397 | ||||||
| chr3:25632600
|
C | A | 125 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(122): Show | 132 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1129-17G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 9/35 | chr3 | 25632600 | ||||||
| chr3:25632650
|
T | C | 2 | a0001c0001t0001g0241a0002c0003t0002g0107 | 2 | NA18612.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1128+43A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 9/35 | chr3 | 25632650 | ||||||
| chr3:25632652
|
C | T | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1128+41G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 9/35 | chr3 | 25632652 | ||||||
| chr3:25632858
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1027-64G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25632858 | ||||||
| chr3:25632904
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1027-110G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25632904 | ||||||
| chr3:25632972
|
T | G | 1 | a0001c0004t0002g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1027-178A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25632972 | ||||||
| chr3:25632993
|
C | T | 149 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(146): Show | 156 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1027-199G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25632993 | ||||||
| chr3:25633020
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1027-226A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25633020 | ||||||
| chr3:25633315
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1027-521A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25633315 | ||||||
| chr3:25633417
|
C | G | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1026+424G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25633417 | ||||||
| chr3:25633457
|
T | C | 1 | a0004c0006t0002g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1026+384A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25633457 | ||||||
| chr3:25633475
|
A | G | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1026+366T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25633475 | ||||||
| chr3:25633688
|
T | C | 1 | a0001c0002t0002g0058 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1026+153A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25633688 | ||||||
| chr3:25633751
|
T | G | 1 | a0002c0003t0002g0111 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1026+90A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 8/35 | chr3 | 25633751 | ||||||
| chr3:25634020
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19070.hp1 | splice_region_variant&intron_variant | LOW | c.853-6T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634020 | ||||||
| chr3:25634146
|
T | C | 159 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0097others(156): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.853-132A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634146 | ||||||
| chr3:25634314
|
G | T | 6 | a0002c0003t0002g0106a0002c0003t0002g0107a0002c0003t0002g0108others(3): Show | 6 | NA18942.hp2 NA18950.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-300C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634314 | ||||||
| chr3:25634418
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0227 | 2 | NA18962.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.853-404G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634418 | ||||||
| chr3:25634453
|
T | C | 152 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(149): Show | 159 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.853-439A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634453 | ||||||
| chr3:25634546
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.853-532G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634546 | ||||||
| chr3:25634608
|
A | G | 10 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(7): Show | 13 | NA18951.hp2 NA18980.hp1 NA18983.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-594T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634608 | ||||||
| chr3:25634615
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.853-601G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634615 | ||||||
| chr3:25634696
|
T | C | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.853-682A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634696 | ||||||
| chr3:25634778
|
C | CA | 23 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(20): Show | 23 | HG01099.hp1 HG01106.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.853-765dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634778 | ||||||
| chr3:25634786
|
A | AC | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-773_853-772ins others(1): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634786 | ||||||
| chr3:25634789
|
A | C | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.853-775T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634789 | ||||||
| chr3:25634791
|
A | AAAC | 132 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0288others(129): Show | 139 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.853-778_853-777ins others(3): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634791 | ||||||
| chr3:25634791
|
A | C | 2 | a0001c0002t0001g0175a0001c0002t0001g0202 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.853-777T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634791 | ||||||
| chr3:25634794
|
A | C | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.853-780T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634794 | ||||||
| chr3:25634795
|
A | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-781T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634795 | ||||||
| chr3:25634797
|
AC | A | 3 | a0001c0001t0001g0166a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | HG01891.hp2 HG02976.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.853-784delG | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634797 | ||||||
| chr3:25634798
|
C | A | 292 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(289): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.853-784G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634798 | ||||||
| chr3:25634799
|
C | A | 15 | a0001c0001t0001g0170a0001c0001t0001g0196a0001c0001t0001g0198others(12): Show | 15 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.853-785G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634799 | ||||||
| chr3:25634806
|
AG | A | 3 | a0001c0002t0002g0027a0001c0002t0002g0038a0001c0002t0002g0039 | 3 | HG02818.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.853-793delC | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634806 | ||||||
| chr3:25634907
|
C | A | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-893G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25634907 | ||||||
| chr3:25635371
|
G | A | 1 | a0001c0002t0002g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.852+565C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25635371 | ||||||
| chr3:25635455
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.852+481A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25635455 | ||||||
| chr3:25635489
|
G | A | 1 | a0004c0006t0002g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.852+447C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25635489 | ||||||
| chr3:25635538
|
G | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.852+398C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25635538 | ||||||
| chr3:25635637
|
G | GA | 153 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0175others(150): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.852+298dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25635637 | ||||||
| chr3:25635683
|
T | C | 1 | a0003c0005t0002g0049 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.852+253A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25635683 | ||||||
| chr3:25635738
|
C | T | 1 | a0001c0002t0002g0066 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.852+198G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25635738 | ||||||
| chr3:25635844
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.852+92C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 7/35 | chr3 | 25635844 | ||||||
| chr3:25636336
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.640-188G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 6/35 | chr3 | 25636336 | ||||||
| chr3:25636437
|
T | C | 131 | a0001c0001t0001g0173a0001c0002t0001g0175a0001c0002t0001g0202others(128): Show | 138 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.640-289A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 6/35 | chr3 | 25636437 | ||||||
| chr3:25636687
|
C | T | 12 | a0001c0002t0001g0175a0001c0002t0001g0202a0001c0002t0002g0002others(9): Show | 13 | HG01070.hp1 HG01071.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.639+528G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 6/35 | chr3 | 25636687 | ||||||
| chr3:25636719
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.639+496A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 6/35 | chr3 | 25636719 | ||||||
| chr3:25636724
|
G | A | 1 | a0001c0002t0002g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.639+491C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 6/35 | chr3 | 25636724 | ||||||
| chr3:25636765
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.639+450G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 6/35 | chr3 | 25636765 | ||||||
| chr3:25636842
|
T | C | 1 | a0001c0002t0002g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.639+373A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 6/35 | chr3 | 25636842 | ||||||
| chr3:25637101
|
G | GA | 61 | a0001c0001t0001g0173a0001c0002t0002g0034a0001c0002t0002g0110others(58): Show | 61 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.639+113dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 6/35 | chr3 | 25637101 | ||||||
| chr3:25637435
|
T | C | 19 | a0002c0003t0002g0099a0002c0003t0002g0100a0002c0003t0002g0115others(16): Show | 19 | HG00673.hp1 HG02015.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.542-123A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637435 | ||||||
| chr3:25637514
|
A | T | 1 | a0001c0001t0001g0007 | 2 | HG01081.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.542-202T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637514 | ||||||
| chr3:25637585
|
C | T | 68 | a0001c0002t0001g0175a0001c0002t0001g0202a0001c0002t0001g0288others(65): Show | 75 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.542-273G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637585 | ||||||
| chr3:25637636
|
C | T | 8 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(5): Show | 8 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.542-324G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637636 | ||||||
| chr3:25637862
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.541+303C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637862 | ||||||
| chr3:25637875
|
A | G | 5 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+290T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637875 | ||||||
| chr3:25637890
|
T | C | 1 | a0001c0002t0002g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.541+275A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637890 | ||||||
| chr3:25637892
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.541+273C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637892 | ||||||
| chr3:25637910
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.541+255A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637910 | ||||||
| chr3:25637983
|
T | A | 159 | a0001c0001t0001g0279a0001c0001t0002g0097a0001c0001t0002g0098others(156): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.541+182A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25637983 | ||||||
| chr3:25638026
|
A | G | 5 | a0004c0006t0002g0086a0004c0006t0002g0088a0004c0006t0002g0089others(2): Show | 5 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.541+139T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25638026 | ||||||
| chr3:25638158
|
A | T | 1 | a0001c0002t0002g0053 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.541+7T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 5/35 | chr3 | 25638158 | ||||||
| chr3:25638314
|
T | TA | 35 | a0001c0001t0001g0008a0001c0001t0001g0160a0001c0001t0001g0164others(32): Show | 36 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(33): Show |
splice_region_variant&intron_variant | LOW | c.396-5dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
T | TAA | 18 | a0001c0001t0001g0161a0001c0001t0001g0170a0001c0001t0001g0182others(15): Show | 18 | HG01243.hp1 HG01346.hp2 HG01884.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.396-6_396-5dupTT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0239 | 1 | HG04199.hp2 | splice_region_variant&intron_variant | LOW | c.396-14_396-5dupTTT others(7): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
T | TAAAAAAA others(4): Show |
3 | a0001c0004t0002g0144a0001c0004t0002g0149a0001c0004t0002g0150 | 3 | HG02559.hp2 HG03130.hp2 HG03471.hp2 |
splice_region_variant&intron_variant | LOW | c.396-15_396-5dupTTT others(8): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
T | TAAAAAAA others(5): Show |
2 | a0001c0004t0002g0145a0001c0004t0002g0147 | 2 | HG03540.hp1 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.396-16_396-5dupTTT others(9): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
T | TAAAAAAA others(8): Show |
1 | a0001c0001t0001g0240 | 1 | HG02056.hp1 | splice_region_variant&intron_variant | LOW | c.396-19_396-5dupTTT others(12): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
T | TAAAAAAA others(9): Show |
1 | a0001c0004t0002g0031 | 1 | HG02717.hp2 | splice_region_variant&intron_variant | LOW | c.396-20_396-5dupTTT others(13): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
T | TAAAAAAA others(11): Show |
1 | a0001c0004t0002g0146 | 1 | HG02145.hp2 | splice_region_variant&intron_variant | LOW | c.396-22_396-5dupTTT others(15): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TA | T | 18 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0179others(15): Show | 18 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.396-5delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAA | T | 7 | a0001c0002t0004g0153a0002c0003t0002g0105a0002c0003t0002g0118others(4): Show | 7 | HG00673.hp1 HG03834.hp1 HG04115.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.396-6_396-5delTT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAA | T | 11 | a0001c0001t0001g0186a0001c0002t0002g0127a0001c0002t0002g0128others(8): Show | 11 | HG01981.hp1 HG02155.hp1 HG02809.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.396-7_396-5delTTT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAA | T | 26 | a0001c0002t0002g0112a0001c0002t0002g0113a0001c0002t0002g0114others(23): Show | 26 | HG00621.hp2 HG00642.hp1 HG01069.hp2 others(23): Show |
splice_region_variant&intron_variant | LOW | c.396-8_396-5delTTTT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAA | T | 13 | a0001c0001t0002g0151a0001c0001t0010g0297a0001c0002t0002g0110others(10): Show | 13 | HG01070.hp2 HG01358.hp1 HG01975.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.396-9_396-5delTTTT others(1): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(2): Show |
T | 14 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0065others(11): Show | 16 | HG00140.hp1 HG01109.hp2 HG01358.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.396-13_396-5delTTT others(6): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(3): Show |
T | 52 | a0001c0001t0001g0172a0001c0001t0001g0196a0001c0002t0001g0202others(49): Show | 57 | HG00423.hp2 HG00639.hp2 HG01071.hp1 others(54): Show |
splice_region_variant&intron_variant | LOW | c.396-14_396-5delTTT others(7): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0002t0001g0175 | 3 | HG01070.hp1 HG01891.hp2 HG02976.hp2 |
splice_region_variant&intron_variant | LOW | c.396-15_396-5delTTT others(8): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(6): Show |
T | 4 | a0001c0001t0001g0012a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 5 | HG01109.hp1 NA18953.hp2 NA19054.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.396-17_396-5delTTT others(10): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(7): Show |
T | 5 | a0001c0001t0001g0213a0001c0001t0001g0284a0001c0001t0001g0287others(2): Show | 5 | HG01255.hp1 HG01346.hp1 HG03654.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.396-18_396-5delTTT others(11): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(8): Show |
T | 6 | a0001c0002t0002g0133a0003c0005t0002g0091a0003c0005t0002g0092others(3): Show | 6 | HG01934.hp2 HG02723.hp2 HG03098.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.396-19_396-5delTTT others(12): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(9): Show |
T | 1 | a0004c0006t0002g0088 | 1 | HG03225.hp1 | splice_region_variant&intron_variant | LOW | c.396-20_396-5delTTT others(13): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(11): Show |
T | 1 | a0002c0003t0002g0123 | 1 | NA18943.hp2 | splice_region_variant&intron_variant | LOW | c.396-22_396-5delTTT others(15): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(12): Show |
T | 2 | a0001c0001t0001g0010a0001c0001t0001g0185 | 3 | NA18942.hp1 NA18975.hp2 NA19091.hp1 |
splice_region_variant&intron_variant | LOW | c.396-23_396-5delTTT others(16): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(14): Show |
T | 1 | a0001c0001t0001g0212 | 1 | NA19010.hp1 | splice_region_variant&intron_variant | LOW | c.396-25_396-5delTTT others(18): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638314
|
TAAAAAAA others(17): Show |
T | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
splice_region_variant&intron_variant | LOW | c.396-28_396-5delTTT others(21): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638314 | ||||||
| chr3:25638320
|
A | T | 1 | a0004c0006t0002g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.396-10T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638320 | ||||||
| chr3:25638321
|
A | T | 2 | a0001c0002t0006g0294a0001c0009t0006g0293 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.396-11T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638321 | ||||||
| chr3:25638322
|
A | T | 1 | a0001c0009t0006g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.396-12T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638322 | ||||||
| chr3:25638325
|
A | T | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.396-15T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638325 | ||||||
| chr3:25638373
|
T | C | 2 | a0001c0002t0002g0071a0001c0002t0002g0074 | 2 | NA19009.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.396-63A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638373 | ||||||
| chr3:25638391
|
T | A | 5 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0048others(2): Show | 5 | HG01243.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-81A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638391 | ||||||
| chr3:25638523
|
T | A | 7 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(4): Show | 7 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.396-213A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638523 | ||||||
| chr3:25638722
|
C | T | 2 | a0002c0003t0002g0105a0002c0003t0002g0120 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.396-412G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638722 | ||||||
| chr3:25638880
|
C | T | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.396-570G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25638880 | ||||||
| chr3:25639033
|
T | A | 1 | a0001c0002t0002g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.396-723A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639033 | ||||||
| chr3:25639196
|
T | C | 7 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(4): Show | 7 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.396-886A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639196 | ||||||
| chr3:25639385
|
T | TG | 158 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0151others(155): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.396-1076_396-1075i others(3): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639385 | ||||||
| chr3:25639460
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0197 | 3 | HG00099.hp1 HG02451.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.396-1150T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639460 | ||||||
| chr3:25639464
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.396-1154G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639464 | ||||||
| chr3:25639542
|
A | G | 156 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0175others(153): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.396-1232T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639542 | ||||||
| chr3:25639689
|
C | T | 3 | a0003c0005t0002g0043a0003c0005t0002g0044a0003c0005t0002g0082 | 3 | HG01243.hp2 HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.396-1379G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639689 | ||||||
| chr3:25639704
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.396-1394A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639704 | ||||||
| chr3:25639770
|
C | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.396-1460G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639770 | ||||||
| chr3:25639927
|
G | A | 3 | a0001c0007t0002g0050a0001c0007t0002g0051a0001c0007t0002g0084 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.396-1617C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639927 | ||||||
| chr3:25639941
|
C | A | 71 | a0001c0002t0001g0175a0001c0002t0001g0202a0001c0002t0001g0288others(68): Show | 78 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.396-1631G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25639941 | ||||||
| chr3:25640060
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.396-1750A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640060 | ||||||
| chr3:25640065
|
C | T | 4 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG00738.hp2 HG01081.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-1755G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640065 | ||||||
| chr3:25640176
|
T | C | 1 | a0002c0003t0002g0103 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.396-1866A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640176 | ||||||
| chr3:25640414
|
T | C | 1 | a0001c0002t0002g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.395+1908A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640414 | ||||||
| chr3:25640531
|
A | C | 1 | a0001c0001t0001g0274 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.395+1791T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640531 | ||||||
| chr3:25640712
|
C | G | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.395+1610G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640712 | ||||||
| chr3:25640752
|
C | CT | 29 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0191others(26): Show | 29 | HG00621.hp1 HG00673.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.395+1569dupA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640752 | ||||||
| chr3:25640752
|
CT | C | 63 | a0001c0001t0001g0173a0001c0001t0001g0183a0001c0001t0001g0195others(60): Show | 63 | HG00639.hp1 HG00642.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.395+1569delA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640752 | ||||||
| chr3:25640752
|
CTTTTTTT others(5): Show |
C | 7 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(4): Show | 7 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.395+1558_395+1569d others(14): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640752 | ||||||
| chr3:25640796
|
C | T | 1 | a0001c0002t0004g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.395+1526G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640796 | ||||||
| chr3:25640815
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.395+1507A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25640815 | ||||||
| chr3:25641072
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.395+1250C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641072 | ||||||
| chr3:25641222
|
TTCA | T | 7 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(4): Show | 7 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.395+1097_395+1099d others(5): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641222 | ||||||
| chr3:25641326
|
C | T | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.395+996G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641326 | ||||||
| chr3:25641365
|
T | C | 5 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.395+957A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641365 | ||||||
| chr3:25641410
|
C | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.395+912G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641410 | ||||||
| chr3:25641536
|
G | GA | 158 | a0001c0001t0001g0173a0001c0001t0002g0097a0001c0001t0002g0098others(155): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.395+785dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641536 | ||||||
| chr3:25641572
|
G | A | 1 | a0001c0002t0002g0131 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.395+750C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641572 | ||||||
| chr3:25641707
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.395+615A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641707 | ||||||
| chr3:25641765
|
T | C | 7 | a0001c0001t0001g0189a0001c0001t0001g0246a0001c0001t0001g0247others(4): Show | 7 | HG00408.hp2 HG02698.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.395+557A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641765 | ||||||
| chr3:25641834
|
C | T | 1 | a0002c0003t0002g0099 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.395+488G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641834 | ||||||
| chr3:25641875
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.395+447A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641875 | ||||||
| chr3:25641945
|
T | C | 2 | a0002c0003t0002g0105a0002c0003t0002g0120 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.395+377A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25641945 | ||||||
| chr3:25642090
|
G | A | 1 | a0001c0002t0002g0079 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.395+232C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25642090 | ||||||
| chr3:25642094
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.395+228A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25642094 | ||||||
| chr3:25642122
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.395+200A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 4/35 | chr3 | 25642122 | ||||||
| chr3:25642439
|
A | C | 68 | a0001c0002t0001g0175a0001c0002t0001g0202a0001c0002t0001g0288others(65): Show | 75 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.332-54T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 3/35 | chr3 | 25642439 | ||||||
| chr3:25642782
|
T | C | 8 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(5): Show | 8 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-397A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 3/35 | chr3 | 25642782 | ||||||
| chr3:25642972
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.332-587A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 3/35 | chr3 | 25642972 | ||||||
| chr3:25643053
|
T | C | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.331+641A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 3/35 | chr3 | 25643053 | ||||||
| chr3:25643080
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.331+614C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 3/35 | chr3 | 25643080 | ||||||
| chr3:25643434
|
T | G | 1 | a0001c0002t0002g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.331+260A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 3/35 | chr3 | 25643434 | ||||||
| chr3:25643583
|
A | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.331+111T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 3/35 | chr3 | 25643583 | ||||||
| chr3:25643669
|
C | A | 1 | a0008c0013t0001g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.331+25G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 3/35 | chr3 | 25643669 | ||||||
| chr3:25643824
|
C | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.241-40G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25643824 | ||||||
| chr3:25644022
|
C | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.241-238G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644022 | ||||||
| chr3:25644098
|
A | C | 62 | a0001c0001t0001g0173a0001c0002t0002g0034a0001c0002t0002g0110others(59): Show | 62 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.241-314T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644098 | ||||||
| chr3:25644101
|
CT | C | 14 | a0001c0001t0001g0267a0001c0007t0002g0050a0001c0007t0002g0051others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.241-318delA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644101 | ||||||
| chr3:25644142
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.241-358A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644142 | ||||||
| chr3:25644252
|
A | T | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.241-468T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644252 | ||||||
| chr3:25644264
|
A | T | 1 | a0002c0003t0002g0099 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.241-480T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644264 | ||||||
| chr3:25644291
|
G | T | 1 | a0004c0006t0002g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.241-507C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644291 | ||||||
| chr3:25644357
|
G | T | 7 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0201others(4): Show | 7 | HG02015.hp1 NA18950.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-573C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644357 | ||||||
| chr3:25644458
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.241-674A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644458 | ||||||
| chr3:25644485
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.241-701C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644485 | ||||||
| chr3:25644577
|
T | G | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+723A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644577 | ||||||
| chr3:25644769
|
A | C | 1 | a0004c0006t0002g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.240+531T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644769 | ||||||
| chr3:25644817
|
T | C | 140 | a0001c0001t0001g0173a0001c0002t0001g0288a0001c0002t0002g0001others(137): Show | 147 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.240+483A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644817 | ||||||
| chr3:25644885
|
C | G | 1 | a0001c0001t0001g0198 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.240+415G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644885 | ||||||
| chr3:25644962
|
A | ATT | 58 | a0001c0001t0001g0173a0001c0002t0002g0110a0001c0002t0002g0112others(55): Show | 58 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.240+336_240+337dup others(2): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644962 | ||||||
| chr3:25644991
|
T | G | 44 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(41): Show | 51 | HG00140.hp1 HG00423.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.240+309A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25644991 | ||||||
| chr3:25645092
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0197 | 3 | HG00099.hp1 HG02451.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.240+208C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25645092 | ||||||
| chr3:25645256
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG00423.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.240+44A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 2/35 | chr3 | 25645256 | ||||||
| chr3:25645544
|
G | T | 1 | a0001c0001t0001g0289 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.70-74C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25645544 | ||||||
| chr3:25645674
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.70-204C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25645674 | ||||||
| chr3:25645894
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.70-424C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25645894 | ||||||
| chr3:25645907
|
G | A | 1 | a0001c0002t0002g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.70-437C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25645907 | ||||||
| chr3:25645926
|
A | AT | 65 | a0001c0001t0001g0008a0001c0001t0001g0173a0001c0001t0001g0195others(62): Show | 66 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-457dupA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25645926 | ||||||
| chr3:25645926
|
A | ATT | 67 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(64): Show | 74 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.70-458_70-457dupAA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25645926 | ||||||
| chr3:25645926
|
A | ATTT | 12 | a0001c0002t0002g0075a0001c0002t0006g0294a0001c0009t0006g0293others(9): Show | 12 | HG01346.hp1 HG01934.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-459_70-457dupAA others(1): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25645926 | ||||||
| chr3:25645978
|
C | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-508G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25645978 | ||||||
| chr3:25645979
|
C | T | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.70-509G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25645979 | ||||||
| chr3:25646464
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.70-994G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25646464 | ||||||
| chr3:25646468
|
G | C | 65 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(62): Show | 72 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.70-998C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25646468 | ||||||
| chr3:25646502
|
G | A | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-1032C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25646502 | ||||||
| chr3:25646536
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.70-1066A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25646536 | ||||||
| chr3:25647102
|
C | T | 1 | a0001c0004t0002g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.70-1632G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25647102 | ||||||
| chr3:25647196
|
T | C | 9 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(6): Show | 9 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-1726A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25647196 | ||||||
| chr3:25647302
|
T | G | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-1832A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25647302 | ||||||
| chr3:25647577
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.70-2107A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25647577 | ||||||
| chr3:25647605
|
A | C | 1 | a0001c0002t0002g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.70-2135T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25647605 | ||||||
| chr3:25647614
|
TA | T | 132 | a0001c0001t0001g0173a0001c0001t0001g0264a0001c0002t0001g0288others(129): Show | 139 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.70-2145delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25647614 | ||||||
| chr3:25647750
|
A | G | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-2280T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25647750 | ||||||
| chr3:25648037
|
GACA | G | 7 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(4): Show | 7 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-2570_70-2568del others(3): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648037 | ||||||
| chr3:25648059
|
T | C | 60 | a0001c0001t0001g0173a0001c0002t0002g0110a0001c0002t0002g0112others(57): Show | 60 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.70-2589A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648059 | ||||||
| chr3:25648395
|
T | G | 1 | a0001c0001t0001g0190 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.70-2925A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648395 | ||||||
| chr3:25648556
|
A | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.70-3086T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648556 | ||||||
| chr3:25648590
|
C | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-3120G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648590 | ||||||
| chr3:25648594
|
C | A | 1 | a0001c0002t0002g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.70-3124G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648594 | ||||||
| chr3:25648638
|
C | CT | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-3169dupA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648638 | ||||||
| chr3:25648681
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.70-3211A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648681 | ||||||
| chr3:25648703
|
C | CA | 4 | a0001c0001t0001g0011a0001c0001t0001g0272a0001c0001t0001g0273others(1): Show | 5 | HG01255.hp2 HG01934.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-3234dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648703 | ||||||
| chr3:25648995
|
G | A | 1 | a0001c0002t0002g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.70-3525C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25648995 | ||||||
| chr3:25649025
|
A | G | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-3555T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649025 | ||||||
| chr3:25649075
|
T | G | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.70-3605A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649075 | ||||||
| chr3:25649350
|
C | T | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG00673.hp2 NA18945.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-3880G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649350 | ||||||
| chr3:25649369
|
T | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-3899A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649369 | ||||||
| chr3:25649470
|
C | A | 1 | a0001c0001t0001g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.70-4000G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649470 | ||||||
| chr3:25649609
|
G | GA | 143 | a0001c0001t0001g0173a0001c0001t0001g0185a0001c0001t0001g0258others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.70-4140dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649609 | ||||||
| chr3:25649609
|
G | GAA | 14 | a0001c0002t0002g0074a0001c0002t0002g0081a0001c0002t0002g0135others(11): Show | 14 | HG01346.hp1 HG01934.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-4141_70-4140dup others(2): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649609 | ||||||
| chr3:25649609
|
GA | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0187a0001c0001t0001g0188others(5): Show | 8 | HG02698.hp1 NA18939.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-4140delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649609 | ||||||
| chr3:25649642
|
T | C | 10 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(7): Show | 13 | NA18951.hp2 NA18980.hp1 NA18983.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-4172A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649642 | ||||||
| chr3:25649717
|
T | G | 1 | a0001c0002t0002g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.70-4247A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649717 | ||||||
| chr3:25649899
|
C | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | NA18939.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.70-4429G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649899 | ||||||
| chr3:25649974
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.70-4504G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649974 | ||||||
| chr3:25649982
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.70-4512G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25649982 | ||||||
| chr3:25650061
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.70-4591A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650061 | ||||||
| chr3:25650128
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.70-4658G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650128 | ||||||
| chr3:25650267
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.70-4797A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650267 | ||||||
| chr3:25650363
|
C | G | 1 | a0001c0001t0001g0185 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.70-4893G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650363 | ||||||
| chr3:25650375
|
G | A | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-4905C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650375 | ||||||
| chr3:25650411
|
T | G | 59 | a0001c0002t0002g0110a0001c0002t0002g0112a0001c0002t0002g0113others(56): Show | 59 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.70-4941A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650411 | ||||||
| chr3:25650505
|
C | T | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.70-5035G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650505 | ||||||
| chr3:25650537
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.70-5067C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650537 | ||||||
| chr3:25650631
|
C | T | 1 | a0001c0002t0002g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.70-5161G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650631 | ||||||
| chr3:25650640
|
C | T | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.70-5170G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650640 | ||||||
| chr3:25650647
|
A | G | 1 | a0002c0003t0002g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.70-5177T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650647 | ||||||
| chr3:25650674
|
T | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-5204A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650674 | ||||||
| chr3:25650830
|
G | T | 14 | a0001c0002t0002g0034a0001c0002t0006g0294a0001c0002t0009g0296others(11): Show | 14 | HG01346.hp1 HG01934.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-5360C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650830 | ||||||
| chr3:25650835
|
G | C | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.70-5365C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650835 | ||||||
| chr3:25650906
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.70-5436A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650906 | ||||||
| chr3:25650910
|
T | C | 1 | a0001c0002t0002g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.70-5440A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650910 | ||||||
| chr3:25650953
|
C | T | 1 | a0001c0004t0002g0030 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.70-5483G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25650953 | ||||||
| chr3:25651012
|
C | T | 14 | a0001c0002t0002g0034a0001c0002t0006g0294a0001c0002t0009g0296others(11): Show | 14 | HG01346.hp1 HG01934.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-5542G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651012 | ||||||
| chr3:25651164
|
C | A | 14 | a0001c0002t0002g0034a0001c0002t0006g0294a0001c0002t0009g0296others(11): Show | 14 | HG01346.hp1 HG01934.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-5694G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651164 | ||||||
| chr3:25651171
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0174a0001c0001t0001g0179others(7): Show | 11 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.70-5701G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651171 | ||||||
| chr3:25651192
|
T | G | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70-5722A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651192 | ||||||
| chr3:25651445
|
T | TA | 71 | a0001c0001t0001g0270a0001c0002t0002g0034a0001c0002t0002g0110others(68): Show | 71 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.70-5976dupT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651445 | ||||||
| chr3:25651445
|
T | TAA | 9 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-5977_70-5976dup others(2): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651445 | ||||||
| chr3:25651518
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-6048G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651518 | ||||||
| chr3:25651744
|
G | A | 125 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(122): Show | 132 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.70-6274C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651744 | ||||||
| chr3:25651864
|
CA | C | 7 | a0001c0001t0001g0176a0001c0001t0001g0280a0001c0001t0002g0151others(4): Show | 7 | HG01070.hp1 HG02015.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-6395delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651864 | ||||||
| chr3:25651955
|
A | G | 1 | a0004c0006t0002g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.70-6485T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25651955 | ||||||
| chr3:25652216
|
C | A | 1 | a0001c0001t0001g0271 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.70-6746G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25652216 | ||||||
| chr3:25652487
|
A | C | 153 | a0001c0001t0001g0173a0001c0002t0001g0288a0001c0002t0002g0001others(150): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.70-7017T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25652487 | ||||||
| chr3:25652541
|
T | C | 1 | a0004c0006t0002g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.70-7071A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25652541 | ||||||
| chr3:25652860
|
G | A | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-7390C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25652860 | ||||||
| chr3:25652906
|
A | G | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.70-7436T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25652906 | ||||||
| chr3:25652915
|
GA | G | 7 | a0002c0003t0002g0102a0002c0003t0002g0103a0002c0003t0002g0104others(4): Show | 7 | HG00408.hp1 HG00621.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-7446delT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25652915 | ||||||
| chr3:25652952
|
C | T | 1 | a0001c0002t0002g0035 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.70-7482G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25652952 | ||||||
| chr3:25652999
|
G | C | 2 | a0001c0002t0002g0034a0001c0002t0009g0296 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.70-7529C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25652999 | ||||||
| chr3:25653037
|
C | T | 156 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0151others(153): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.70-7567G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25653037 | ||||||
| chr3:25653050
|
A | T | 1 | a0001c0004t0002g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.70-7580T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25653050 | ||||||
| chr3:25653135
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0272a0001c0001t0001g0273others(1): Show | 5 | HG01255.hp2 HG01934.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-7665C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25653135 | ||||||
| chr3:25653406
|
T | G | 1 | a0010c0015t0002g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-7936A>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25653406 | ||||||
| chr3:25653562
|
T | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-8092A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25653562 | ||||||
| chr3:25653610
|
T | C | 8 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(5): Show | 8 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-8140A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25653610 | ||||||
| chr3:25653635
|
G | A | 59 | a0001c0002t0002g0110a0001c0002t0002g0112a0001c0002t0002g0113others(56): Show | 59 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.70-8165C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25653635 | ||||||
| chr3:25653667
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.70-8197G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25653667 | ||||||
| chr3:25653872
|
T | C | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.70-8402A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25653872 | ||||||
| chr3:25654072
|
T | C | 157 | a0001c0001t0001g0173a0001c0001t0002g0097a0001c0001t0002g0098others(154): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.70-8602A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25654072 | ||||||
| chr3:25654076
|
T | C | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.70-8606A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25654076 | ||||||
| chr3:25654181
|
T | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG00423.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.70-8711A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25654181 | ||||||
| chr3:25654329
|
A | G | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.70-8859T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25654329 | ||||||
| chr3:25654381
|
G | C | 2 | a0001c0002t0002g0034a0001c0002t0009g0296 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.70-8911C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25654381 | ||||||
| chr3:25654466
|
T | C | 4 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295others(1): Show | 4 | HG02145.hp1 HG02572.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-8996A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25654466 | ||||||
| chr3:25654662
|
A | G | 14 | a0001c0002t0002g0034a0001c0002t0006g0294a0001c0002t0009g0296others(11): Show | 14 | HG01346.hp1 HG01934.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-9192T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25654662 | ||||||
| chr3:25654897
|
T | A | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.69+9332A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25654897 | ||||||
| chr3:25654920
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.69+9309C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25654920 | ||||||
| chr3:25655016
|
G | T | 1 | a0001c0001t0001g0173 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.69+9213C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655016 | ||||||
| chr3:25655115
|
C | T | 6 | a0001c0002t0002g0027a0001c0002t0002g0035a0001c0002t0002g0036others(3): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+9114G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655115 | ||||||
| chr3:25655307
|
G | C | 1 | a0001c0004t0002g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.69+8922C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655307 | ||||||
| chr3:25655375
|
C | G | 157 | a0001c0001t0001g0173a0001c0001t0002g0097a0001c0001t0002g0098others(154): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.69+8854G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655375 | ||||||
| chr3:25655379
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.69+8850A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655379 | ||||||
| chr3:25655475
|
G | T | 1 | a0001c0001t0001g0172 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.69+8754C>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655475 | ||||||
| chr3:25655495
|
T | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.69+8734A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655495 | ||||||
| chr3:25655876
|
G | C | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69+8353C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655876 | ||||||
| chr3:25655898
|
A | G | 6 | a0004c0006t0002g0086a0004c0006t0002g0088a0004c0006t0002g0089others(3): Show | 6 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+8331T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655898 | ||||||
| chr3:25655914
|
G | A | 2 | a0003c0005t0002g0091a0003c0005t0002g0092 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.69+8315C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25655914 | ||||||
| chr3:25656815
|
A | G | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69+7414T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25656815 | ||||||
| chr3:25656884
|
A | C | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.69+7345T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25656884 | ||||||
| chr3:25657030
|
G | C | 66 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(63): Show | 73 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.69+7199C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657030 | ||||||
| chr3:25657078
|
G | A | 1 | a0003c0005t0002g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.69+7151C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657078 | ||||||
| chr3:25657162
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.69+7067A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657162 | ||||||
| chr3:25657213
|
G | A | 77 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(74): Show | 84 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.69+7016C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657213 | ||||||
| chr3:25657491
|
C | T | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+6738G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657491 | ||||||
| chr3:25657629
|
A | ACT | 9 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(6): Show | 9 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+6598_69+6599dup others(2): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657629 | ||||||
| chr3:25657700
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.69+6529T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657700 | ||||||
| chr3:25657787
|
C | G | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+6442G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657787 | ||||||
| chr3:25657819
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.69+6410A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657819 | ||||||
| chr3:25657831
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.69+6398C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657831 | ||||||
| chr3:25657858
|
G | C | 80 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+6371C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657858 | ||||||
| chr3:25657866
|
CCCGG | C | 80 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+6359_69+6362del others(4): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657866 | ||||||
| chr3:25657868
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.69+6361G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657868 | ||||||
| chr3:25657875
|
A | C | 80 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+6354T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657875 | ||||||
| chr3:25657877
|
C | T | 80 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+6352G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657877 | ||||||
| chr3:25657897
|
TAAAAATA others(159): Show |
T | 80 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+6166_69+6331del | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25657897 | ||||||
| chr3:25658056
|
G | A | 1 | a0002c0003t0003g0021 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.69+6173C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658056 | ||||||
| chr3:25658060
|
C | CAAAAAAA others(1): Show |
7 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+6161_69+6168dup others(8): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658060 | ||||||
| chr3:25658060
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0002g0151a0001c0001t0010g0297a0001c0002t0002g0140 | 3 | HG03225.hp2 NA18522.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.69+6168_69+6169ins others(19): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658060 | ||||||
| chr3:25658070
|
A | AAAAAAAA others(13): Show |
7 | a0001c0002t0002g0136a0001c0002t0002g0137a0001c0002t0002g0138others(4): Show | 7 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+6158_69+6159ins others(20): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658070 | ||||||
| chr3:25658070
|
A | AAAAAAAA others(12): Show |
24 | a0001c0002t0002g0121a0001c0002t0002g0122a0001c0002t0002g0124others(21): Show | 24 | HG00642.hp1 HG00673.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.69+6158_69+6159ins others(19): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658070 | ||||||
| chr3:25658070
|
A | AAAAAAAA others(11): Show |
29 | a0001c0002t0002g0110a0001c0002t0002g0112a0001c0002t0002g0113others(26): Show | 29 | HG00408.hp1 HG00621.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.69+6158_69+6159ins others(18): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658070 | ||||||
| chr3:25658070
|
A | AAAAAAAA others(11): Show |
1 | a0011c0016t0002g0101 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.69+6158_69+6159ins others(18): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658070 | ||||||
| chr3:25658070
|
A | T | 80 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+6159T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658070 | ||||||
| chr3:25658072
|
A | C | 80 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+6157T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658072 | ||||||
| chr3:25658218
|
C | T | 3 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295 | 3 | HG02145.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.69+6011G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658218 | ||||||
| chr3:25658240
|
T | C | 80 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+5989A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658240 | ||||||
| chr3:25658249
|
A | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01517.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.69+5980T>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658249 | ||||||
| chr3:25658655
|
T | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+5574A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658655 | ||||||
| chr3:25658893
|
T | C | 10 | a0001c0004t0002g0030a0001c0004t0002g0031a0001c0004t0002g0096others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+5336A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25658893 | ||||||
| chr3:25659271
|
T | TC | 5 | a0001c0002t0006g0294a0001c0009t0006g0293a0001c0009t0006g0295others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+4957dupG | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25659271 | ||||||
| chr3:25659423
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.69+4806T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25659423 | ||||||
| chr3:25659518
|
T | A | 68 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(65): Show | 75 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.69+4711A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25659518 | ||||||
| chr3:25659584
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69+4645G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25659584 | ||||||
| chr3:25659624
|
G | C | 1 | a0001c0002t0009g0296 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.69+4605C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25659624 | ||||||
| chr3:25659703
|
T | C | 80 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+4526A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25659703 | ||||||
| chr3:25659884
|
C | A | 1 | a0001c0002t0002g0083 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.69+4345G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25659884 | ||||||
| chr3:25659943
|
A | G | 1 | a0001c0007t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.69+4286T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25659943 | ||||||
| chr3:25660280
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.69+3949C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660280 | ||||||
| chr3:25660288
|
T | A | 95 | a0001c0001t0002g0151a0001c0001t0010g0297a0001c0002t0001g0288others(92): Show | 102 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.69+3941A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660288 | ||||||
| chr3:25660376
|
T | A | 1 | a0001c0001t0001g0279 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69+3853A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660376 | ||||||
| chr3:25660404
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.69+3825G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660404 | ||||||
| chr3:25660554
|
A | G | 156 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0151others(153): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.69+3675T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660554 | ||||||
| chr3:25660597
|
C | A | 296 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(293): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.69+3632G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660597 | ||||||
| chr3:25660606
|
G | A | 156 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0151others(153): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.69+3623C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660606 | ||||||
| chr3:25660631
|
T | C | 3 | a0005c0008t0005g0156a0005c0008t0005g0157a0005c0008t0005g0158 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.69+3598A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660631 | ||||||
| chr3:25660772
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.69+3457A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660772 | ||||||
| chr3:25660986
|
G | A | 7 | a0003c0005t0002g0091a0003c0005t0002g0092a0004c0006t0002g0086others(4): Show | 7 | HG01346.hp1 HG01934.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+3243C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660986 | ||||||
| chr3:25660998
|
A | AT | 80 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0286others(77): Show | 87 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+3230dupA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660998 | ||||||
| chr3:25660998
|
A | ATT | 8 | a0001c0001t0002g0151a0001c0001t0010g0297a0001c0002t0002g0026others(5): Show | 8 | HG01934.hp2 HG02145.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+3229_69+3230dup others(2): Show |
TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660998 | ||||||
| chr3:25660998
|
AT | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0281a0001c0001t0001g0282others(5): Show | 9 | HG01069.hp2 HG02922.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+3230delA | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25660998 | ||||||
| chr3:25661159
|
C | G | 70 | a0001c0002t0001g0288a0001c0002t0002g0001a0001c0002t0002g0002others(67): Show | 77 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.69+3070G>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25661159 | ||||||
| chr3:25661279
|
G | A | 1 | a0001c0002t0002g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.69+2950C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25661279 | ||||||
| chr3:25661289
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69+2940C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25661289 | ||||||
| chr3:25661300
|
G | A | 8 | a0001c0004t0002g0096a0001c0004t0002g0144a0001c0004t0002g0145others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+2929C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25661300 | ||||||
| chr3:25661464
|
T | C | 1 | a0001c0017t0001g0285 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.69+2765A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25661464 | ||||||
| chr3:25661477
|
C | A | 1 | a0001c0001t0010g0297 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.69+2752G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25661477 | ||||||
| chr3:25661671
|
C | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | NA18953.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.69+2558G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25661671 | ||||||
| chr3:25661909
|
T | C | 156 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0151others(153): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.69+2320A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25661909 | ||||||
| chr3:25662149
|
C | T | 94 | a0001c0001t0002g0151a0001c0001t0010g0297a0001c0002t0002g0001others(91): Show | 101 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.69+2080G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25662149 | ||||||
| chr3:25662178
|
C | T | 1 | a0002c0003t0002g0099 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.69+2051G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25662178 | ||||||
| chr3:25662463
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.69+1766G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25662463 | ||||||
| chr3:25662783
|
A | C | 8 | a0001c0004t0002g0096a0001c0004t0002g0144a0001c0004t0002g0145others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+1446T>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25662783 | ||||||
| chr3:25662952
|
C | T | 1 | a0001c0002t0002g0025 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.69+1277G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25662952 | ||||||
| chr3:25663008
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.69+1221A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663008 | ||||||
| chr3:25663035
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.69+1194T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663035 | ||||||
| chr3:25663054
|
G | C | 2 | a0001c0001t0002g0151a0001c0001t0010g0297 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69+1175C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663054 | ||||||
| chr3:25663098
|
G | A | 59 | a0001c0002t0002g0110a0001c0002t0002g0112a0001c0002t0002g0113others(56): Show | 59 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.69+1131C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663098 | ||||||
| chr3:25663149
|
T | C | 9 | a0001c0001t0002g0151a0001c0004t0002g0096a0001c0004t0002g0144others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+1080A>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663149 | ||||||
| chr3:25663312
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+917C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663312 | ||||||
| chr3:25663512
|
G | A | 61 | a0001c0001t0002g0151a0001c0001t0010g0297a0001c0002t0002g0110others(58): Show | 61 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.69+717C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663512 | ||||||
| chr3:25663748
|
A | G | 94 | a0001c0001t0002g0151a0001c0001t0010g0297a0001c0002t0002g0001others(91): Show | 101 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.69+481T>C | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663748 | ||||||
| chr3:25663825
|
T | A | 8 | a0001c0001t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(5): Show | 8 | NA18942.hp2 NA18944.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+404A>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663825 | ||||||
| chr3:25663826
|
C | T | 8 | a0001c0001t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(5): Show | 8 | NA18942.hp2 NA18944.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+403G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663826 | ||||||
| chr3:25663941
|
GAA | G | 82 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0003others(79): Show | 89 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.69+286_69+287delTT | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25663941 | ||||||
| chr3:25664068
|
C | A | 1 | a0001c0002t0002g0143 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.69+161G>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25664068 | ||||||
| chr3:25664130
|
G | A | 8 | a0001c0001t0002g0151a0001c0004t0002g0144a0001c0004t0002g0145others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+99C>T | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25664130 | ||||||
| chr3:25664187
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.69+42G>A | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25664187 | ||||||
| chr3:25664212
|
G | C | 1 | a0001c0001t0001g0292 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.69+17C>G | TOP2B | ENSG00000077097.17 | transcript | ENST00000264331.9 | protein_coding | 1/35 | chr3 | 25664212 |