| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130579446-130579683 | Common:6; Rare:101 | ||||
| chr9:130693592-130693800 | Rare:69 | ||||
| chr9:130835059-130835386 | Common:9; Rare:88 | ||||
| chr9:131125379-131125637 | Common:3; Rare:116 | ||||
| chr9:131502865-131503033 | Rare:59; Clinvar:3 | ||||
| chr9:131531182-131531396 | Common:10; Rare:96 | ||||
| chr9:132354919-132355186 | Common:3; Rare:88 | ||||
| chr9:132406813-132406894 | Rare:30 | ||||
| chr9:132669930-132670046 | Common:1; Rare:55 | ||||
| chr9:132878272-132878414 | Common:1; Rare:56 | ||||
| chr9:133336120-133336314 | Common:1; Rare:85 | ||||
| chr9:133348037-133348253 | Common:3; Rare:80 | ||||
| chr9:133356436-133356636 | Common:1; Rare:96; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375995-133376366 | Common:2; Rare:134 | ||||
| chr9:133418052-133418312 | Common:3; Rare:54 |