Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:19854782-19855065 | Common:2; Rare:105 | ||||
chr22:19941715-19942116 | Common:2; Rare:116; Clinvar:5; Clinvar (benign):4 | ||||
chr22:20117124-20117600 | Common:3; Rare:152 | ||||
chr22:20495786-20495994 | Common:2; Rare:78 | ||||
chr22:20507509-20507675 | Rare:64 | ||||
chr22:20858748-20859093 | Common:5; Rare:171; Clinvar:3; Clinvar (benign):3 | ||||
chr22:20982223-20982361 | Common:1; Rare:31; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr22:23894087-23894846 | Common:8; Rare:264; Clinvar:1 | ||||
chr22:24244545-24244618 | Rare:27 | ||||
chr22:24555030-24555444 | Common:4; Rare:149 | ||||
chr22:24555617-24556045 | Rare:135 | ||||
chr22:26512436-26512567 | Common:2; Rare:58 | ||||
chr22:27919184-27919504 | Common:5; Rare:142 | ||||
chr22:28741789-28742082 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):3 | ||||
chr22:28742407-28742712 | Common:1; Rare:75 |