Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:39319594-39319838 | Common:3; Rare:100 | ||||
chr22:40044543-40044852 | Common:2; Rare:73 | ||||
chr22:40346441-40346664 | Rare:102; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr22:40636668-40637012 | Common:2; Rare:96 | ||||
chr22:40856924-40857126 | Common:1; Rare:74; Clinvar:1 | ||||
chr22:41446795-41446958 | Rare:65 | ||||
chr22:41468638-41468773 | Common:2; Rare:37 | ||||
chr22:41621006-41621368 | Common:7; Rare:134 | ||||
chr22:41832909-41833225 | Common:3; Rare:106 | ||||
chr22:41947114-41947206 | Rare:29 | ||||
chr22:42070761-42070956 | Common:2; Rare:43 | ||||
chr22:42090730-42090945 | Common:1; Rare:79; Clinvar (pathogenic):1 | ||||
chr22:42614858-42615246 | Common:3; Rare:161 | ||||
chr22:43015093-43015384 | Common:2; Rare:120 | ||||
chr22:43955303-43955560 | Common:3; Rare:77 |