| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:27573723-27573980 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384471-32384732 | Common:1; Rare:93 | ||||
| chr9:32526171-32526344 | Common:4; Rare:50 | ||||
| chr9:32573041-32573219 | Common:2; Rare:66 | ||||
| chr9:33001518-33001721 | Common:2; Rare:115; Clinvar (benign):4 | ||||
| chr9:33025035-33025400 | Common:7; Rare:143 | ||||
| chr9:33076583-33076877 | Common:2; Rare:95 | ||||
| chr9:33166763-33166956 | Rare:64; Clinvar:3 | ||||
| chr9:33167318-33167582 | Rare:99 | ||||
| chr9:33264736-33265100 | Rare:96 | ||||
| chr9:33290255-33290578 | Common:3; Rare:109 | ||||
| chr9:33290856-33290956 | Rare:25 | ||||
| chr9:33393983-33394319 | Common:4; Rare:60 | ||||
| chr9:33401235-33401687 | Common:3; Rare:98 | ||||
| chr9:33401976-33402031 | Common:1; Rare:15 |