| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132406801-132406893 | Rare:32 | ||||
| chr9:132669936-132670051 | Common:1; Rare:54 | ||||
| chr9:132878277-132878410 | Common:1; Rare:49 | ||||
| chr9:132878806-132878954 | Rare:27 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133030920-133031041 | Rare:47 | ||||
| chr9:133336133-133336351 | Common:1; Rare:88 | ||||
| chr9:133348025-133348268 | Common:3; Rare:97 | ||||
| chr9:133356458-133356618 | Common:1; Rare:76; Clinvar (benign):2 | ||||
| chr9:133375999-133376370 | Common:1; Rare:133 | ||||
| chr9:133418040-133418296 | Common:4; Rare:51 | ||||
| chr9:134641547-134641771 | Common:1; Rare:66 | ||||
| chr9:135499848-135499960 | Common:3; Rare:31 | ||||
| chr9:136410350-136410670 | Common:6; Rare:132 | ||||
| chr9:136849590-136849778 | Common:1; Rare:69 |