Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:41800411-41800694 | Common:3; Rare:83 | ||||
chr22:41832840-41833295 | Common:3; Rare:159 | ||||
chr22:41947089-41947196 | Rare:38 | ||||
chr22:42070538-42070956 | Common:3; Rare:98; Clinvar:1 | ||||
chr22:42079511-42079763 | Common:2; Rare:67 | ||||
chr22:42090658-42090945 | Common:2; Rare:129; Clinvar (pathogenic):1 | ||||
chr22:42519753-42519874 | Common:1; Rare:57 | ||||
chr22:42614853-42615244 | Common:3; Rare:159 | ||||
chr22:42649297-42649482 | Common:1; Rare:69 | ||||
chr22:42720813-42720956 | Rare:45 | ||||
chr22:43089325-43089496 | Common:3; Rare:55 | ||||
chr22:43955303-43955566 | Common:3; Rare:80 | ||||
chr22:44024175-44024384 | Common:1; Rare:67 | ||||
chr22:44026282-44026340 | Rare:14 | ||||
chr22:45163766-45164003 | Common:2; Rare:92 |