Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:19447684-19447850 | Common:2; Rare:66 | ||||
chr22:20020944-20021139 | Common:1; Rare:61 | ||||
chr22:20079935-20080253 | Common:1; Rare:104 | ||||
chr22:20117240-20117651 | Common:4; Rare:135 | ||||
chr22:20320009-20320158 | Common:1; Rare:50 | ||||
chr22:20495775-20495904 | Common:1; Rare:48 | ||||
chr22:20858696-20859095 | Common:6; Rare:201; Clinvar:3; Clinvar (benign):3 | ||||
chr22:20982204-20982312 | Common:2; Rare:20; Clinvar (benign):2 | ||||
chr22:21002106-21002208 | Common:3; Rare:33 | ||||
chr22:21938079-21938311 | Rare:81 | ||||
chr22:24555892-24556040 | Rare:46 | ||||
chr22:26483775-26484078 | Common:9; Rare:137; Clinvar:5; Clinvar (benign):2 | ||||
chr22:26512447-26512542 | Common:1; Rare:46 | ||||
chr22:27919195-27919470 | Common:4; Rare:123 | ||||
chr22:28741798-28742082 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):1 |