Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:37953597-37953784 | Rare:81 | ||||
chr22:37984506-37984765 | Common:1; Rare:58 | ||||
chr22:38681821-38682092 | Common:2; Rare:109 | ||||
chr22:39319579-39319768 | Common:3; Rare:86 | ||||
chr22:40346441-40346556 | Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
chr22:40856957-40857159 | Rare:90; Clinvar:3 | ||||
chr22:41468633-41469019 | Common:2; Rare:88 | ||||
chr22:41469042-41469152 | Rare:41 | ||||
chr22:41621018-41621386 | Common:7; Rare:134 | ||||
chr22:41832879-41833152 | Common:3; Rare:90 | ||||
chr22:41947032-41947198 | Common:1; Rare:59 | ||||
chr22:42079616-42079769 | Common:1; Rare:50 | ||||
chr22:42090745-42090953 | Common:1; Rare:69 | ||||
chr22:42614850-42615244 | Common:3; Rare:161 | ||||
chr22:43089327-43089496 | Common:3; Rare:54 |