Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7153 |
| ensemblid | ENSG00000131747.15 |
| hgncid | 11989 |
| symbol | TOP2A |
| name | DNA topoisomerase II alpha |
| refseq_nuc | NM_001067.4 |
| refseq_prot | NP_001058.2 |
| ensembl_nuc | ENST00000423485.6 |
| ensembl_prot | ENSP00000411532.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 40388525 |
| end | 40417896 |
| strand | - |
| ver | v1.2 |
| region | chr17:40388525-40417896 |
| region5000 | chr17:40383525-40422896 |
| regionname0 | TOP2A_chr17_40388525_40417896 |
| regionname5000 | TOP2A_chr17_40383525_40422896 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1531 | 238 | 66 | 45 | 87 | 10 | 28 | 68 | TOP2A_chr17_40383525_40422896 | TOP2A | MEVSP others(1526): Show |
chr17 | 40383525 | 40422896 |
| a0002 | 0/0 | 1531 | 14 | 10 | 3 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | MEVSP others(1526): Show |
chr17 | 40383525 | 40422896 |
| a0003 | 0/0 | 1531 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | MEVSP others(1526): Show |
chr17 | 40383525 | 40422896 |
| a0004 | 0/0 | 1531 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | MEVSP others(1526): Show |
chr17 | 40383525 | 40422896 |
| a0005 | 0/0 | 1531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | MEVSP others(1526): Show |
chr17 | 40383525 | 40422896 |
| a0006 | 0/0 | 1531 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | MEVSP others(1526): Show |
chr17 | 40383525 | 40422896 |
| a0007 | 0/0 | 1531 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | MEVSP others(1526): Show |
chr17 | 40383525 | 40422896 |
| a0008 | 0/0 | 1531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | MEVSP others(1526): Show |
chr17 | 40383525 | 40422896 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4593 | 235 | 63 | 45 | 87 | 10 | 28 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0001c0005 | 0/0 | 4593 | 2 | 2 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0001c0008 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0002c0002 | 0/0 | 4593 | 6 | 6 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0002c0003 | 0/0 | 4593 | 3 | 1 | 1 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0002c0004 | 0/0 | 4593 | 3 | 2 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0002c0006 | 0/0 | 4593 | 2 | 1 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0003c0010 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0004c0011 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0005c0013 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0006c0009 | 0/0 | 4593 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0007c0007 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 | ||
| a0008c0012 | 0/0 | 4593 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | ATGGA others(4588): Show |
chr17 | 40383525 | 40422896 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5695 | 205 | 59 | 39 | 74 | 7 | 24 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0001c0001t0002 | 0/0 | 5695 | 14 | 2 | 5 | 0 | 3 | 4 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0001c0001t0003 | 0/0 | 5695 | 12 | 0 | 0 | 12 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0001c0001t0006 | 0/0 | 5695 | 2 | 2 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0001c0001t0007 | 0/0 | 5695 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0001c0001t0008 | 0/0 | 5695 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0001c0005t0001 | 0/0 | 5695 | 2 | 2 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0001c0008t0001 | 0/0 | 5695 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0002c0002t0001 | 0/0 | 5695 | 6 | 6 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0002c0003t0004 | 0/0 | 5695 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0002c0003t0005 | 0/0 | 5695 | 2 | 0 | 1 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0002c0004t0001 | 0/0 | 5695 | 3 | 2 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0002c0006t0001 | 0/0 | 5695 | 2 | 1 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0003c0010t0001 | 0/0 | 5695 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0004c0011t0001 | 0/0 | 5695 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0005c0013t0001 | 0/0 | 5695 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0006c0009t0001 | 0/0 | 5695 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0007c0007t0001 | 0/0 | 5695 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| a0008c0012t0004 | 0/0 | 5695 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | AACCG others(5690): Show |
chr17 | 40383525 | 40422896 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 28 | 2 | 9 | 11 | 1 | 4 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0002 | 0/0 | 21 | 3 | 6 | 9 | 1 | 2 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0003g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0001c0008t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0002t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0003t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0003t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0003t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0004t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0006t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0002c0006t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0003c0010t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0004c0011t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0005c0013t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0006c0009t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0007c0007t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| a0008c0012t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00099 | hp2 | a0002 | c0003 | t0005 | g0156 | EUR | GBR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0123 | EUR | FIN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0138 | EAS | CHS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | CHS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00733 | hp1 | a0003 | c0010 | t0001 | g0124 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01081 | hp1 | a0002 | c0006 | t0001 | g0152 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01109 | hp2 | a0002 | c0004 | t0001 | g0161 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0114 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0116 | EUR | IBS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01943 | hp2 | a0004 | c0011 | t0001 | g0034 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02148 | hp1 | a0002 | c0003 | t0005 | g0155 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02622 | hp2 | a0005 | c0013 | t0001 | g0153 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02647 | hp1 | a0001 | c0008 | t0001 | g0062 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02886 | hp2 | a0002 | c0003 | t0004 | g0158 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02970 | hp1 | a0001 | c0005 | t0001 | g0061 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0113 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18612 | hp1 | a0006 | c0009 | t0001 | g0068 | EAS | CHB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | LWK | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | LWK | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA20129 | hp2 | a0002 | c0006 | t0001 | g0149 | AFR | ASW | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA20752 | hp2 | a0007 | c0007 | t0001 | g0029 | EUR | TSI | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0073 | AFR | ACB | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03471 | hp1 | a0002 | c0004 | t0001 | g0160 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| HG06807 | hp2 | a0002 | c0004 | t0001 | g0159 | AFR | USA | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| NA21309 | hp2 | a0008 | c0012 | t0004 | g0157 | AFR | LWK | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0064 | REF | REF | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TOP2A_chr17_40383525_40422896 | TOP2A | chr17 | 40383525 | 40422896 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:40389572 | C | A | 3 | a0002 a0005 a0008 |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
missense_variant | MODERATE | c.4543G>T | p.Ala1515Ser | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 35/35 | 4648/5695 | 4543/4596 | 1515/1531 | chr17 | 40389572 | |||
| chr17:40389972 | G | C | 1 | a0004 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.4460C>G | p.Thr1487Arg | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 34/35 | 4565/5695 | 4460/4596 | 1487/1531 | chr17 | 40389972 | |||
| chr17:40391616 | C | T | 3 | a0002 a0005 a0008 |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
missense_variant | MODERATE | c.4157G>A | p.Gly1386Asp | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/35 | 4262/5695 | 4157/4596 | 1386/1531 | chr17 | 40391616 | |||
| chr17:40392684 | T | C | 1 | a0008 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.3865A>G | p.Lys1289Glu | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 30/35 | 3970/5695 | 3865/4596 | 1289/1531 | chr17 | 40392684 | |||
| chr17:40396414 | C | G | 1 | a0003 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.3589G>C | p.Gly1197Arg | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 28/35 | 3694/5695 | 3589/4596 | 1197/1531 | chr17 | 40396414 | |||
| chr17:40400861 | G | T | 1 | a0006 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.2653C>A | p.Pro885Thr | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 21/35 | 2758/5695 | 2653/4596 | 885/1531 | chr17 | 40400861 | |||
| chr17:40411739 | T | C | 1 | a0005 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.869A>G | p.His290Arg | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 8/35 | 974/5695 | 869/4596 | 290/1531 | chr17 | 40411739 | |||
| chr17:40416422 | C | A | 1 | a0007 | 1 | NA20752.hp2 | missense_variant&splice_region_variant | MODERATE | c.268G>T | p.Val90Phe | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 373/5695 | 268/4596 | 90/1531 | chr17 | 40416422 | |||
| chr17:40416425 | G | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.265C>A | p.Leu89Ile | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 370/5695 | 265/4596 | 89/1531 | chr17 | 40416425 | |||
| chr17:40416427 | A | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.263T>A | p.Ile88Asn | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 368/5695 | 263/4596 | 88/1531 | chr17 | 40416427 | |||
| chr17:40416429 | C | G | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.261G>C | p.Glu87Asp | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 366/5695 | 261/4596 | 87/1531 | chr17 | 40416429 | |||
| chr17:40416431 | C | A | 1 | a0007 | 1 | NA20752.hp2 | stop_gained | HIGH | c.259G>T | p.Glu87* | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 364/5695 | 259/4596 | 87/1531 | chr17 | 40416431 | |||
| chr17:40416432 | A | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.258T>A | p.Asp86Glu | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 363/5695 | 258/4596 | 86/1531 | chr17 | 40416432 | |||
| chr17:40416434 | C | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.256G>A | p.Asp86Asn | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 361/5695 | 256/4596 | 86/1531 | chr17 | 40416434 | |||
| chr17:40416436 | A | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.254T>A | p.Phe85Tyr | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 359/5695 | 254/4596 | 85/1531 | chr17 | 40416436 | |||
| chr17:40416442 | T | A | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.248A>T | p.Lys83Ile | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 353/5695 | 248/4596 | 83/1531 | chr17 | 40416442 | |||
| chr17:40416449 | A | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.241T>A | p.Leu81Met | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 346/5695 | 241/4596 | 81/1531 | chr17 | 40416449 | |||
| chr17:40416451 | C | A | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.239G>T | p.Gly80Val | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 344/5695 | 239/4596 | 80/1531 | chr17 | 40416451 | |||
| chr17:40416454 | G | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.236C>A | p.Pro79His | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 341/5695 | 236/4596 | 79/1531 | chr17 | 40416454 | |||
| chr17:40416455 | G | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.235C>A | p.Pro79Thr | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 340/5695 | 235/4596 | 79/1531 | chr17 | 40416455 | |||
| chr17:40416461 | A | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.229T>A | p.Phe77Ile | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 334/5695 | 229/4596 | 77/1531 | chr17 | 40416461 | |||
| chr17:40416464 | T | A | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.226A>T | p.Thr76Ser | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 331/5695 | 226/4596 | 76/1531 | chr17 | 40416464 | |||
| chr17:40416468 | T | A | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.222A>T | p.Glu74Asp | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 327/5695 | 222/4596 | 74/1531 | chr17 | 40416468 | |||
| chr17:40416470 | C | A | 1 | a0007 | 1 | NA20752.hp2 | stop_gained | HIGH | c.220G>T | p.Glu74* | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 325/5695 | 220/4596 | 74/1531 | chr17 | 40416470 | |||
| chr17:40416485 | C | G | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.205G>C | p.Gly69Arg | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 310/5695 | 205/4596 | 69/1531 | chr17 | 40416485 | |||
| chr17:40416487 | A | G | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.203T>C | p.Val68Ala | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 308/5695 | 203/4596 | 68/1531 | chr17 | 40416487 | |||
| chr17:40416488 | C | T | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.202G>A | p.Val68Ile | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 307/5695 | 202/4596 | 68/1531 | chr17 | 40416488 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:40392277 | A | C | 2 | a0002c0006 a0005c0013 |
3 | HG01081.hp1 HG02622.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.4029T>G | p.Thr1343Thr | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 31/35 | 4134/5695 | 4029/4596 | 1343/1531 | chr17 | 40392277 | |||
| chr17:40392334 | T | G | 6 | a0002c0002 a0002c0003 a0002c0004 others(3): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
synonymous_variant | LOW | c.3972A>C | p.Thr1324Thr | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 31/35 | 4077/5695 | 3972/4596 | 1324/1531 | chr17 | 40392334 | |||
| chr17:40400281 | T | C | 3 | a0002c0002 a0002c0006 a0005c0013 |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
synonymous_variant | LOW | c.2928A>G | p.Lys976Lys | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 23/35 | 3033/5695 | 2928/4596 | 976/1531 | chr17 | 40400281 | |||
| chr17:40406856 | C | T | 1 | a0001c0005 | 2 | HG02559.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.1713G>A | p.Glu571Glu | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 14/35 | 1818/5695 | 1713/4596 | 571/1531 | chr17 | 40406856 | |||
| chr17:40412819 | T | C | 1 | a0002c0004 | 3 | HG01109.hp2 HG03471.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.729A>G | p.Ala243Ala | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 7/35 | 834/5695 | 729/4596 | 243/1531 | chr17 | 40412819 | |||
| chr17:40412846 | A | G | 1 | a0001c0008 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.702T>C | p.Asp234Asp | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 7/35 | 807/5695 | 702/4596 | 234/1531 | chr17 | 40412846 | |||
| chr17:40416438 | G | T | 1 | a0007c0007 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.252C>A | p.Ile84Ile | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 357/5695 | 252/4596 | 84/1531 | chr17 | 40416438 | |||
| chr17:40416444 | G | A | 1 | a0007c0007 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.246C>T | p.Tyr82Tyr | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 351/5695 | 246/4596 | 82/1531 | chr17 | 40416444 | |||
| chr17:40416447 | C | T | 1 | a0007c0007 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.243G>A | p.Leu81Leu | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 348/5695 | 243/4596 | 81/1531 | chr17 | 40416447 | |||
| chr17:40416453 | A | T | 1 | a0007c0007 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.237T>A | p.Pro79Pro | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 342/5695 | 237/4596 | 79/1531 | chr17 | 40416453 | |||
| chr17:40416465 | G | A | 1 | a0007c0007 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.225C>T | p.Val75Val | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/35 | 330/5695 | 225/4596 | 75/1531 | chr17 | 40416465 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:40388941 | C | T | 1 | a0001c0001t0002 | 14 | HG00323.hp1 HG00642.hp1 HG01123.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 35/35 | 578 | chr17 | 40388941 | ||||||
| chr17:40388990 | C | T | 1 | a0001c0001t0003 | 12 | HG00558.hp1 NA18747.hp2 NA18941.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*529G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 35/35 | 529 | chr17 | 40388990 | ||||||
| chr17:40389050 | T | C | 1 | a0002c0003t0005 | 2 | HG00099.hp2 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*469A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 35/35 | 469 | chr17 | 40389050 | ||||||
| chr17:40389099 | T | C | 1 | a0001c0001t0007 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 35/35 | 420 | chr17 | 40389099 | ||||||
| chr17:40389125 | G | A | 1 | a0001c0001t0006 | 2 | HG03225.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*394C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 35/35 | 394 | chr17 | 40389125 | ||||||
| chr17:40389212 | C | T | 2 | a0002c0003t0004 a0008c0012t0004 |
2 | HG02886.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*307G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 35/35 | 307 | chr17 | 40389212 | ||||||
| chr17:40389254 | T | A | 1 | a0001c0001t0008 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*265A>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 35/35 | 265 | chr17 | 40389254 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:40389773 | A | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0111 |
2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.4468-126T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 34/34 | chr17 | 40389773 | |||||||
| chr17:40390249 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.4268-85A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390249 | |||||||
| chr17:40390334 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02572.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4268-170C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390334 | |||||||
| chr17:40390349 | C | T | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.4268-185G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390349 | |||||||
| chr17:40390517 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4268-353A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390517 | |||||||
| chr17:40390617 | A | C | 1 | a0002c0004t0001g0161 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4268-453T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390617 | |||||||
| chr17:40390624 | A | ATT | 10 | a0002c0002t0001g0009 a0002c0002t0001g0154 a0002c0003t0004g0158 others(7): Show |
13 | HG01081.hp1 HG01109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.4268-462_4268-461d others(4): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390624 | |||||||
| chr17:40390624 | AT | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0039 others(4): Show |
9 | HG00735.hp1 HG02615.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.4268-461delA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390624 | |||||||
| chr17:40390666 | C | T | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.4268-502G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390666 | |||||||
| chr17:40390739 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4268-575A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390739 | |||||||
| chr17:40390752 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4268-588G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390752 | |||||||
| chr17:40390818 | T | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(107): Show |
166 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.4268-654A>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40390818 | |||||||
| chr17:40391038 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4267+468T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40391038 | |||||||
| chr17:40391112 | G | A | 1 | a0002c0003t0004g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4267+394C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40391112 | |||||||
| chr17:40391125 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0054 |
3 | HG02486.hp1 HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4267+381T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40391125 | |||||||
| chr17:40391168 | GT | G | 3 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 |
6 | HG02451.hp2 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4267+337delA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40391168 | |||||||
| chr17:40391276 | G | C | 2 | a0002c0003t0004g0158 a0008c0012t0004g0157 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4267+230C>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40391276 | |||||||
| chr17:40391325 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0054 |
3 | HG02486.hp1 HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4267+181C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40391325 | |||||||
| chr17:40391416 | G | A | 11 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(8): Show |
14 | HG01081.hp1 HG01109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.4267+90C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40391416 | |||||||
| chr17:40391447 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4267+59T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 33/34 | chr17 | 40391447 | |||||||
| chr17:40391911 | G | A | 1 | a0001c0001t0008g0114 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.4132+157C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 32/34 | chr17 | 40391911 | |||||||
| chr17:40391977 | G | A | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.4132+91C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 32/34 | chr17 | 40391977 | |||||||
| chr17:40392750 | T | C | 2 | a0002c0004t0001g0159 a0002c0004t0001g0160 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3812-13A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40392750 | |||||||
| chr17:40392878 | T | C | 2 | a0001c0005t0001g0061 a0001c0005t0001g0073 |
2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3812-141A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40392878 | |||||||
| chr17:40393013 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3812-276G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40393013 | |||||||
| chr17:40393585 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3812-848C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40393585 | |||||||
| chr17:40393688 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0106 |
2 | HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3812-951C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40393688 | |||||||
| chr17:40393745 | T | C | 1 | a0002c0003t0004g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3812-1008A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40393745 | |||||||
| chr17:40393799 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3812-1062G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40393799 | |||||||
| chr17:40393842 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3812-1105C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40393842 | |||||||
| chr17:40393883 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3812-1146G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40393883 | |||||||
| chr17:40393987 | C | T | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.3812-1250G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40393987 | |||||||
| chr17:40394065 | C | CA | 14 | a0001c0001t0001g0010 a0002c0002t0001g0009 a0002c0002t0001g0151 others(11): Show |
19 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.3812-1329dupT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40394065 | |||||||
| chr17:40394065 | CA | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
161 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.3812-1329delT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40394065 | |||||||
| chr17:40394176 | G | C | 1 | a0002c0003t0004g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3811+1273C>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40394176 | |||||||
| chr17:40394199 | C | CAAATAGG others(15): Show |
13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3811+1249_3811+125 others(26): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40394199 | |||||||
| chr17:40394450 | A | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0118 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3811+999T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40394450 | |||||||
| chr17:40394632 | C | T | 2 | a0002c0004t0001g0159 a0002c0004t0001g0160 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3811+817G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40394632 | |||||||
| chr17:40394772 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02572.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3811+677T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40394772 | |||||||
| chr17:40394843 | A | C | 1 | a0005c0013t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3811+606T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40394843 | |||||||
| chr17:40395022 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3811+427G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395022 | |||||||
| chr17:40395055 | C | T | 3 | a0002c0004t0001g0159 a0002c0004t0001g0160 a0002c0004t0001g0161 |
3 | HG01109.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3811+394G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395055 | |||||||
| chr17:40395059 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3811+390G>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395059 | |||||||
| chr17:40395085 | C | T | 2 | a0001c0005t0001g0061 a0001c0005t0001g0073 |
2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3811+364G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395085 | |||||||
| chr17:40395096 | A | G | 1 | a0008c0012t0004g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3811+353T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395096 | |||||||
| chr17:40395119 | C | T | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3811+330G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395119 | |||||||
| chr17:40395276 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3811+173A>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395276 | |||||||
| chr17:40395281 | C | CA | 25 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0037 others(22): Show |
30 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.3811+167dupT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395281 | |||||||
| chr17:40395281 | C | CAA | 8 | a0001c0001t0001g0072 a0001c0001t0001g0098 a0001c0001t0001g0132 others(5): Show |
8 | HG00099.hp2 HG00323.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3811+166_3811+167d others(4): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395281 | |||||||
| chr17:40395362 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3811+87C>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395362 | |||||||
| chr17:40395381 | G | C | 3 | a0002c0004t0001g0159 a0002c0004t0001g0160 a0002c0004t0001g0161 |
3 | HG01109.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3811+68C>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 29/34 | chr17 | 40395381 | |||||||
| chr17:40395666 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3721-127A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 28/34 | chr17 | 40395666 | |||||||
| chr17:40395985 | CT | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
194 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.3720+297delA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 28/34 | chr17 | 40395985 | |||||||
| chr17:40396062 | CTCTGCCT others(19): Show |
C | 1 | a0001c0001t0001g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3720+195_3720+220d others(28): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 28/34 | chr17 | 40396062 | |||||||
| chr17:40396072 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0028 |
3 | HG01123.hp1 HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.3720+211G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 28/34 | chr17 | 40396072 | |||||||
| chr17:40396082 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3720+201G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 28/34 | chr17 | 40396082 | |||||||
| chr17:40396140 | C | T | 1 | a0002c0004t0001g0161 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3720+143G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 28/34 | chr17 | 40396140 | |||||||
| chr17:40396170 | A | C | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3720+113T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 28/34 | chr17 | 40396170 | |||||||
| chr17:40396588 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3538-123A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396588 | |||||||
| chr17:40396713 | G | A | 1 | a0002c0004t0001g0161 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3538-248C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396713 | |||||||
| chr17:40396755 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3538-290A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396755 | |||||||
| chr17:40396756 | A | G | 5 | a0002c0003t0004g0158 a0002c0004t0001g0159 a0002c0004t0001g0160 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3538-291T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396756 | |||||||
| chr17:40396793 | C | T | 2 | a0002c0002t0001g0009 a0002c0002t0001g0154 |
5 | HG02451.hp2 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3538-328G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396793 | |||||||
| chr17:40396858 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0118 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3538-393T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396858 | |||||||
| chr17:40396900 | G | GT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(9): Show |
13 | HG01168.hp2 HG01169.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.3538-436dupA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396900 | |||||||
| chr17:40396900 | G | T | 2 | a0002c0004t0001g0159 a0002c0004t0001g0160 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3538-435C>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396900 | |||||||
| chr17:40396922 | C | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0024 others(15): Show |
26 | HG00438.hp2 HG01109.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.3538-457G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396922 | |||||||
| chr17:40396944 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02572.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3538-479T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40396944 | |||||||
| chr17:40397033 | C | T | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3538-568G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40397033 | |||||||
| chr17:40397037 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3538-572G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40397037 | |||||||
| chr17:40397086 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3538-621G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40397086 | |||||||
| chr17:40397285 | CT | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(103): Show |
162 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.3538-821delA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40397285 | |||||||
| chr17:40397285 | CTT | C | 17 | a0001c0001t0001g0059 a0001c0001t0001g0142 a0001c0001t0001g0150 others(14): Show |
20 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3538-822_3538-821d others(4): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40397285 | |||||||
| chr17:40397532 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3537+1026G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40397532 | |||||||
| chr17:40397778 | A | T | 3 | a0002c0004t0001g0159 a0002c0004t0001g0160 a0002c0004t0001g0161 |
3 | HG01109.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3537+780T>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40397778 | |||||||
| chr17:40397778 | AT | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0056 others(7): Show |
12 | HG00099.hp2 HG02148.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.3537+779delA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40397778 | |||||||
| chr17:40398036 | C | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0026 others(17): Show |
30 | HG00733.hp1 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.3537+522G>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40398036 | |||||||
| chr17:40398110 | C | CT | 10 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0053 others(7): Show |
10 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.3537+447dupA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40398110 | |||||||
| chr17:40398110 | CT | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0047 a0001c0001t0001g0056 others(10): Show |
16 | HG00099.hp2 HG01070.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3537+447delA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40398110 | |||||||
| chr17:40398140 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG01192.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.3537+418C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40398140 | |||||||
| chr17:40398299 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02572.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3537+259A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40398299 | |||||||
| chr17:40398300 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3537+258A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40398300 | |||||||
| chr17:40398500 | G | T | 1 | a0002c0004t0001g0161 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3537+58C>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 27/34 | chr17 | 40398500 | |||||||
| chr17:40398954 | A | G | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.3289-17T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 25/34 | chr17 | 40398954 | |||||||
| chr17:40399239 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3197-108C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399239 | |||||||
| chr17:40399305 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3197-174A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399305 | |||||||
| chr17:40399331 | A | ATATGAGG others(1): Show |
135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
195 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.3197-201_3197-200i others(10): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399331 | |||||||
| chr17:40399463 | G | A | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3197-332C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399463 | |||||||
| chr17:40399464 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3197-333G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399464 | |||||||
| chr17:40399504 | G | GT | 12 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(9): Show |
15 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.3196+367_3196+368i others(3): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399504 | |||||||
| chr17:40399506 | C | T | 12 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(9): Show |
15 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.3196+366G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399506 | |||||||
| chr17:40399552 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0091 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3196+320A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399552 | |||||||
| chr17:40399589 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0103 |
3 | HG03098.hp1 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3196+283T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399589 | |||||||
| chr17:40399743 | C | T | 1 | a0008c0012t0004g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3196+129G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399743 | |||||||
| chr17:40399744 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0118 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3196+128C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 24/34 | chr17 | 40399744 | |||||||
| chr17:40400165 | T | G | 1 | a0001c0001t0001g0093 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3000+44A>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 23/34 | chr17 | 40400165 | |||||||
| chr17:40400188 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3000+21A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 23/34 | chr17 | 40400188 | |||||||
| chr17:40400502 | C | T | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2799+27G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 22/34 | chr17 | 40400502 | |||||||
| chr17:40400518 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
195 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.2799+11A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 22/34 | chr17 | 40400518 | |||||||
| chr17:40401272 | G | A | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2433-191C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40401272 | |||||||
| chr17:40401316 | G | A | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2433-235C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40401316 | |||||||
| chr17:40401450 | C | T | 1 | a0001c0001t0003g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2433-369G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40401450 | |||||||
| chr17:40401662 | T | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(107): Show |
166 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.2433-581A>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40401662 | |||||||
| chr17:40401748 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2433-667C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40401748 | |||||||
| chr17:40401753 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2433-672T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40401753 | |||||||
| chr17:40401788 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2433-707C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40401788 | |||||||
| chr17:40401810 | T | C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433-729A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40401810 | |||||||
| chr17:40402044 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2432+862A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40402044 | |||||||
| chr17:40402066 | G | C | 1 | a0001c0005t0001g0061 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2432+840C>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40402066 | |||||||
| chr17:40402186 | C | T | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2432+720G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40402186 | |||||||
| chr17:40402377 | G | T | 1 | a0001c0001t0002g0020 | 2 | HG01255.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2432+529C>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40402377 | |||||||
| chr17:40402534 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2432+372A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40402534 | |||||||
| chr17:40402791 | C | T | 1 | a0001c0005t0001g0073 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2432+115G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 20/34 | chr17 | 40402791 | |||||||
| chr17:40403062 | GA | G | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2284-9delT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40403062 | |||||||
| chr17:40403084 | A | C | 1 | a0002c0003t0004g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2284-30T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40403084 | |||||||
| chr17:40403309 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-255T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40403309 | |||||||
| chr17:40403509 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
6 | NA18948.hp2 NA19062.hp2 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.2284-455A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40403509 | |||||||
| chr17:40403541 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2284-487G>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40403541 | |||||||
| chr17:40403901 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2283+251A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40403901 | |||||||
| chr17:40403935 | C | T | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2283+217G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40403935 | |||||||
| chr17:40404052 | A | C | 1 | a0001c0001t0001g0045 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2283+100T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40404052 | |||||||
| chr17:40404136 | T | A | 2 | a0001c0005t0001g0061 a0001c0005t0001g0073 |
2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2283+16A>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40404136 | |||||||
| chr17:40404143 | T | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0100 |
3 | HG01123.hp2 HG02683.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2283+9A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 19/34 | chr17 | 40404143 | |||||||
| chr17:40405046 | A | G | 1 | a0003c0010t0001g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1954-163T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405046 | |||||||
| chr17:40405071 | C | T | 1 | a0007c0007t0001g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1954-188G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405071 | |||||||
| chr17:40405114 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1954-231A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405114 | |||||||
| chr17:40405457 | G | GT | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): Show |
152 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.1954-575dupA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405457 | |||||||
| chr17:40405457 | G | GTT | 15 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0051 others(12): Show |
18 | HG01168.hp1 HG01168.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1954-576_1954-575d others(4): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405457 | |||||||
| chr17:40405601 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1954-718G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405601 | |||||||
| chr17:40405686 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1953+698C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405686 | |||||||
| chr17:40405701 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02572.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1953+683G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405701 | |||||||
| chr17:40405742 | T | C | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1953+642A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405742 | |||||||
| chr17:40405813 | C | G | 1 | a0001c0001t0001g0074 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1953+571G>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405813 | |||||||
| chr17:40405927 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1953+457G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40405927 | |||||||
| chr17:40406117 | T | A | 1 | a0005c0013t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1953+267A>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40406117 | |||||||
| chr17:40406259 | A | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02572.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1953+125T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40406259 | |||||||
| chr17:40406292 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1953+92A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40406292 | |||||||
| chr17:40406375 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1953+9G>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 16/34 | chr17 | 40406375 | |||||||
| chr17:40406976 | C | T | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1627-34G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 13/34 | chr17 | 40406976 | |||||||
| chr17:40407004 | C | G | 1 | a0001c0001t0001g0019 | 2 | HG00735.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1627-62G>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 13/34 | chr17 | 40407004 | |||||||
| chr17:40407046 | C | T | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
7 | HG01361.hp2 HG04199.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.1627-104G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 13/34 | chr17 | 40407046 | |||||||
| chr17:40407458 | C | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
194 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1626+91G>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 13/34 | chr17 | 40407458 | |||||||
| chr17:40407833 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0103 others(3): Show |
12 | HG02451.hp1 HG02647.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.1500+134A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 12/34 | chr17 | 40407833 | |||||||
| chr17:40408229 | T | C | 1 | a0002c0002t0001g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1343-105A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 11/34 | chr17 | 40408229 | |||||||
| chr17:40408337 | A | G | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1342+155T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 11/34 | chr17 | 40408337 | |||||||
| chr17:40408355 | C | T | 1 | a0004c0011t0001g0034 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1342+137G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 11/34 | chr17 | 40408355 | |||||||
| chr17:40408420 | C | T | 3 | a0002c0006t0001g0149 a0002c0006t0001g0152 a0005c0013t0001g0153 |
3 | HG01081.hp1 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1342+72G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 11/34 | chr17 | 40408420 | |||||||
| chr17:40408804 | C | G | 1 | a0002c0004t0001g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1204-174G>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40408804 | |||||||
| chr17:40408874 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1204-244A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40408874 | |||||||
| chr17:40408926 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1204-296C>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40408926 | |||||||
| chr17:40409194 | C | CA | 15 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
16 | HG00323.hp1 HG00323.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1204-565dupT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409194 | |||||||
| chr17:40409194 | C | CAAAAAAA others(3): Show |
1 | a0002c0003t0005g0155 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1204-574_1204-565d others(12): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409194 | |||||||
| chr17:40409194 | C | CAAAAAAA others(5): Show |
2 | a0002c0004t0001g0159 a0008c0012t0004g0157 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1204-576_1204-565d others(14): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409194 | |||||||
| chr17:40409194 | C | CAAAAAAA others(6): Show |
3 | a0002c0003t0004g0158 a0002c0004t0001g0160 a0002c0004t0001g0161 |
3 | HG01109.hp2 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1204-577_1204-565d others(15): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409194 | |||||||
| chr17:40409194 | CA | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.1204-565delT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409194 | |||||||
| chr17:40409194 | CAA | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0065 a0001c0001t0001g0066 others(6): Show |
13 | HG01081.hp1 HG01943.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204-566_1204-565d others(4): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409194 | |||||||
| chr17:40409268 | T | G | 1 | a0003c0010t0001g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1204-638A>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409268 | |||||||
| chr17:40409298 | CCTGGGAG others(17): Show |
C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1204-692_1204-669d others(26): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409298 | |||||||
| chr17:40409374 | C | CA | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1204-745dupT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409374 | |||||||
| chr17:40409645 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1204-1015C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409645 | |||||||
| chr17:40409779 | C | CA | 10 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0125 others(7): Show |
11 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1204-1150dupT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409779 | |||||||
| chr17:40409822 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1204-1192C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409822 | |||||||
| chr17:40409949 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1203+1160T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40409949 | |||||||
| chr17:40410075 | GAGACTCT others(12): Show |
G | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1203+1015_1203+103 others(23): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40410075 | |||||||
| chr17:40410281 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1203+828C>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40410281 | |||||||
| chr17:40410471 | A | C | 1 | a0001c0001t0001g0033 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1203+638T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40410471 | |||||||
| chr17:40410638 | T | C | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1203+471A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40410638 | |||||||
| chr17:40410729 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1203+380A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40410729 | |||||||
| chr17:40410756 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1203+353C>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40410756 | |||||||
| chr17:40410934 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1203+175G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40410934 | |||||||
| chr17:40411066 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0006g0135 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1203+43A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40411066 | |||||||
| chr17:40411082 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1203+27A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 10/34 | chr17 | 40411082 | |||||||
| chr17:40411879 | G | T | 2 | a0002c0003t0005g0155 a0002c0003t0005g0156 |
2 | HG00099.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.790-61C>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 7/34 | chr17 | 40411879 | |||||||
| chr17:40411997 | C | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
195 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.790-179G>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 7/34 | chr17 | 40411997 | |||||||
| chr17:40412272 | G | A | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.790-454C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 7/34 | chr17 | 40412272 | |||||||
| chr17:40412642 | T | TCAAACAA others(1): Show |
4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0139 others(1): Show |
4 | HG00438.hp1 HG00438.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+109_789+116dup others(8): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 7/34 | chr17 | 40412642 | |||||||
| chr17:40412642 | TCAAA | T | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.789+113_789+116del others(4): Show |
TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 7/34 | chr17 | 40412642 | |||||||
| chr17:40413315 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.479-23G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 5/34 | chr17 | 40413315 | |||||||
| chr17:40413380 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.479-88A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 5/34 | chr17 | 40413380 | |||||||
| chr17:40413390 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.478+90A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 5/34 | chr17 | 40413390 | |||||||
| chr17:40413812 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.333-187T>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40413812 | |||||||
| chr17:40413825 | C | T | 1 | a0001c0005t0001g0061 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.333-200G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40413825 | |||||||
| chr17:40413916 | C | T | 1 | a0001c0001t0002g0017 | 2 | HG01361.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.333-291G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40413916 | |||||||
| chr17:40414087 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.333-462C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414087 | |||||||
| chr17:40414131 | A | AT | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.333-507dupA | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414131 | |||||||
| chr17:40414542 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.333-917A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414542 | |||||||
| chr17:40414582 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.333-957G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414582 | |||||||
| chr17:40414728 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.333-1103G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414728 | |||||||
| chr17:40414854 | C | CA | 14 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0048 others(11): Show |
20 | HG01175.hp1 HG02451.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.332+1150dupT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414854 | |||||||
| chr17:40414854 | CA | C | 8 | a0001c0001t0001g0059 a0002c0003t0004g0158 a0002c0003t0005g0155 others(5): Show |
8 | HG00099.hp2 HG01109.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.332+1150delT | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414854 | |||||||
| chr17:40414979 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02572.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.332+1026T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414979 | |||||||
| chr17:40414985 | C | A | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.332+1020G>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414985 | |||||||
| chr17:40414985 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.332+1020G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40414985 | |||||||
| chr17:40415123 | C | T | 1 | a0002c0002t0001g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.332+882G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40415123 | |||||||
| chr17:40415147 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0054 |
3 | HG02486.hp1 HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.332+858G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40415147 | |||||||
| chr17:40415244 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.332+761G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40415244 | |||||||
| chr17:40415300 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.332+705G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40415300 | |||||||
| chr17:40415454 | C | T | 1 | a0002c0003t0005g0155 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.332+551G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40415454 | |||||||
| chr17:40415555 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.332+450A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40415555 | |||||||
| chr17:40415971 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.332+34C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 4/34 | chr17 | 40415971 | |||||||
| chr17:40416072 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18966.hp2 | splice_region_variant&intron_variant | LOW | c.269-4T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416072 | |||||||
| chr17:40416114 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
194 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.269-46C>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416114 | |||||||
| chr17:40416128 | C | T | 6 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(3): Show |
9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.269-60G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416128 | |||||||
| chr17:40416225 | C | G | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.269-157G>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416225 | |||||||
| chr17:40416411 | G | T | 1 | a0007c0007t0001g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.268+11C>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416411 | |||||||
| chr17:40416412 | A | T | 1 | a0007c0007t0001g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.268+10T>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416412 | |||||||
| chr17:40416413 | T | A | 1 | a0007c0007t0001g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.268+9A>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416413 | |||||||
| chr17:40416417 | C | T | 1 | a0007c0007t0001g0029 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.268+5G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416417 | |||||||
| chr17:40416418 | T | A | 1 | a0007c0007t0001g0029 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.268+4A>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416418 | |||||||
| chr17:40416419 | C | T | 1 | a0007c0007t0001g0029 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.268+3G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416419 | |||||||
| chr17:40416421 | C | T | 1 | a0007c0007t0001g0029 | 1 | NA20752.hp2 | splice_donor_variant&intron_variant | HIGH | c.268+1G>A | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 3/34 | chr17 | 40416421 | |||||||
| chr17:40416992 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(10): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.22-97A>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 1/34 | chr17 | 40416992 | |||||||
| chr17:40417117 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.22-222C>G | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 1/34 | chr17 | 40417117 | |||||||
| chr17:40417224 | A | G | 1 | a0001c0001t0001g0014 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.22-329T>C | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 1/34 | chr17 | 40417224 | |||||||
| chr17:40417440 | C | A | 12 | a0002c0002t0001g0009 a0002c0002t0001g0151 a0002c0002t0001g0154 others(9): Show |
15 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.21+331G>T | TOP2A | ENSG00000131747.15 | transcript | ENST00000423485.6 | protein_coding | 1/34 | chr17 | 40417440 |