| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133030475-133030752 | Common:4; Rare:74 | ||||
| chr9:133030920-133031020 | Rare:35 | ||||
| chr9:133336133-133336341 | Common:1; Rare:82 | ||||
| chr9:133348037-133348281 | Common:3; Rare:104 | ||||
| chr9:133356443-133356614 | Common:1; Rare:80; Clinvar (benign):2 | ||||
| chr9:133375959-133376366 | Common:3; Rare:146 | ||||
| chr9:133417788-133418325 | Common:5; Rare:165 | ||||
| chr9:133459946-133460058 | Common:1; Rare:49 | ||||
| chr9:133738296-133738446 | Common:2; Rare:44 | ||||
| chr9:133739877-133740062 | Rare:31 | ||||
| chr9:134371804-134371991 | Rare:47 | ||||
| chr9:136410417-136410686 | Common:6; Rare:120 | ||||
| chr9:136849634-136849874 | Common:1; Rare:78 | ||||
| chr9:136944592-136944991 | Common:2; Rare:146 | ||||
| chr9:136945820-136946219 | Common:10; Rare:184 |