Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:35301674-35301711 | Rare:8 | ||||
chr22:36288725-36289152 | Common:2; Rare:124; Clinvar:3; Clinvar (benign):6 | ||||
chr22:37807252-37807254 | |||||
chr22:41529276-41529440 | Rare:46 | ||||
chr22:42210786-42210978 | Rare:56 | ||||
chr22:42269653-42269920 | Common:1; Rare:91 | ||||
chr22:42587926-42588172 | Common:3; Rare:45 | ||||
chr22:43163137-43163334 | Common:2; Rare:41 | ||||
chr22:43174262-43174571 | Common:2; Rare:132 | ||||
chr22:45130561-45130668 | Rare:34 | ||||
chr22:45162147-45162445 | Common:1; Rare:70 | ||||
chr22:45163216-45163274 | Rare:16 | ||||
chr22:46052802-46052941 | Common:1; Rare:27 | ||||
chr22:46069860-46070093 | Rare:53 | ||||
chr22:46080056-46080369 | Common:1; Rare:97 |