Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:40177737-40178011 | Rare:81 | ||||
chr22:40346424-40346585 | Rare:75; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr22:40370438-40370675 | Rare:90 | ||||
chr22:40636659-40637045 | Common:2; Rare:103 | ||||
chr22:40856413-40857169 | Common:3; Rare:310; Clinvar:4 | ||||
chr22:40951015-40951424 | Common:2; Rare:139 | ||||
chr22:40951600-40951848 | Common:2; Rare:73 | ||||
chr22:41091379-41091837 | Common:6; Rare:168 | ||||
chr22:41205139-41205366 | Rare:73 | ||||
chr22:41286142-41286424 | Common:2; Rare:91 | ||||
chr22:41381274-41381455 | Common:4; Rare:63 | ||||
chr22:41446778-41446986 | Rare:87 | ||||
chr22:41468628-41468798 | Common:2; Rare:45 | ||||
chr22:41468980-41469175 | Rare:69 | ||||
chr22:41544293-41544897 | Common:12; Rare:191 |