| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129835217-129835475 | Common:2; Rare:104 | ||||
| chr9:130053877-130053929 | Common:1; Rare:18 | ||||
| chr9:130579428-130579641 | Common:3; Rare:64 | ||||
| chr9:130693502-130693806 | Rare:89 | ||||
| chr9:132406801-132406885 | Rare:27 | ||||
| chr9:132669939-132670035 | Common:1; Rare:48 | ||||
| chr9:132878279-132878418 | Common:1; Rare:54 | ||||
| chr9:133030447-133030742 | Common:4; Rare:78 | ||||
| chr9:133336128-133336290 | Common:1; Rare:63 | ||||
| chr9:133348061-133348258 | Common:2; Rare:79 | ||||
| chr9:133356425-133356607 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375999-133376340 | Common:1; Rare:125 | ||||
| chr9:133417939-133418094 | Common:1; Rare:42 | ||||
| chr9:135499856-135499966 | Common:3; Rare:30 | ||||
| chr9:136410417-136410664 | Common:6; Rare:107 |