Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:34651989-34652201 | Rare:64 | ||||
chr9:34665381-34665646 | Rare:86 | ||||
chr9:34990105-34990273 | Rare:39 | ||||
chr9:35102803-35103198 | Common:1; Rare:123 | ||||
chr9:35489924-35490144 | Common:3; Rare:63 | ||||
chr9:35646835-35646951 | Rare:24 | ||||
chr9:35657841-35658371 | Common:9; Rare:441; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
chr9:35732083-35732334 | Common:2; Rare:70 | ||||
chr9:35732342-35732684 | Common:3; Rare:94 | ||||
chr9:35748989-35749369 | Common:2; Rare:141 | ||||
chr9:35814976-35815294 | Rare:79 | ||||
chr9:36190737-36190988 | Common:1; Rare:84 | ||||
chr9:36258386-36258599 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
chr9:36572791-36572938 | Rare:40 | ||||
chr9:37120174-37120623 | Common:2; Rare:141 |