Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:41446790-41446924 | Rare:49 | ||||
chr22:41621008-41621365 | Common:7; Rare:132 | ||||
chr22:41832909-41833131 | Common:3; Rare:71 | ||||
chr22:41947095-41947267 | Rare:61 | ||||
chr22:42090730-42090991 | Common:1; Rare:98; Clinvar (pathogenic):1 | ||||
chr22:42614946-42615246 | Common:3; Rare:125 | ||||
chr22:42649333-42649479 | Common:1; Rare:56 | ||||
chr22:43955303-43955556 | Common:3; Rare:75 | ||||
chr22:45163677-45164015 | Common:4; Rare:120 | ||||
chr22:46053795-46053895 | Rare:36 | ||||
chr22:46250278-46250423 | Common:2; Rare:50 | ||||
chr22:46296750-46296915 | Rare:53 | ||||
chr22:46335621-46335786 | Common:4; Rare:73; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr22:46762526-46762663 | Common:3; Rare:45 | ||||
chr22:49918425-49918675 | Common:1; Rare:85 |