| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35657854-35658376 | Common:8; Rare:436; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35689702-35690123 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35731964-35732334 | Common:2; Rare:93 | ||||
| chr9:35732373-35732704 | Common:3; Rare:84 | ||||
| chr9:35748954-35749377 | Common:2; Rare:152 | ||||
| chr9:35812250-35812326 | Rare:24 | ||||
| chr9:35814975-35815294 | Rare:80 | ||||
| chr9:35829068-35829269 | Common:1; Rare:53 | ||||
| chr9:36136624-36136781 | Common:2; Rare:52 | ||||
| chr9:36190637-36190989 | Common:1; Rare:109 | ||||
| chr9:36258395-36258646 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572772-36572934 | Rare:44 | ||||
| chr9:37120183-37120618 | Common:2; Rare:134 | ||||
| chr9:37422580-37422730 | Common:2; Rare:76 | ||||
| chr9:37485737-37486000 | Common:1; Rare:93 |