Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:25696814-25697050 | Common:3; Rare:68 | ||||
chr20:32109685-32109740 | Rare:28 | ||||
chr20:32207724-32207917 | Common:1; Rare:72 | ||||
chr20:33401504-33401589 | Rare:22 | ||||
chr20:35699308-35699466 | Rare:55; Clinvar (benign):3 | ||||
chr20:35742175-35742595 | Common:5; Rare:127 | ||||
chr20:37289570-37289669 | Common:1; Rare:29 | ||||
chr20:38033416-38033612 | Common:1; Rare:70 | ||||
chr20:44210785-44211095 | Common:4; Rare:108 | ||||
chr20:44966370-44966523 | Rare:59 | ||||
chr20:45857357-45857704 | Common:3; Rare:88 | ||||
chr20:45891258-45891384 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):1 | ||||
chr20:49278038-49278244 | Rare:57 | ||||
chr20:50958496-50958830 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):3 | ||||
chr20:56392163-56392397 | Rare:66 |