Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:39319594-39319779 | Common:3; Rare:83 | ||||
chr22:40044527-40044828 | Common:2; Rare:72 | ||||
chr22:40346454-40346556 | Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
chr22:40636668-40637022 | Common:2; Rare:98 | ||||
chr22:40856438-40856754 | Rare:141 | ||||
chr22:40856768-40857158 | Common:2; Rare:150; Clinvar:3 | ||||
chr22:41446773-41446980 | Rare:87 | ||||
chr22:41468980-41469148 | Rare:51 | ||||
chr22:41621024-41621368 | Common:7; Rare:130 | ||||
chr22:41800390-41800631 | Common:2; Rare:68 | ||||
chr22:41832909-41833145 | Common:3; Rare:77 | ||||
chr22:42090686-42091001 | Common:2; Rare:139; Clinvar (pathogenic):1 | ||||
chr22:42614854-42615248 | Common:3; Rare:164 | ||||
chr22:42649311-42649482 | Common:1; Rare:67 | ||||
chr22:43015104-43015384 | Common:2; Rare:116 |