| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128275895-128276319 | Common:5; Rare:187 | ||||
| chr9:128322417-128322619 | Common:1; Rare:56 | ||||
| chr9:128371196-128371433 | Rare:91 | ||||
| chr9:128422844-128423216 | Common:2; Rare:100 | ||||
| chr9:128455917-128456244 | Common:2; Rare:106 | ||||
| chr9:128460440-128460606 | Common:1; Rare:42 | ||||
| chr9:128492429-128492805 | Rare:60 | ||||
| chr9:128504414-128504747 | Common:2; Rare:98; Clinvar:3 | ||||
| chr9:128552388-128552693 | Rare:114; Clinvar:6; Clinvar (benign):3 | ||||
| chr9:128552953-128553110 | Rare:43 | ||||
| chr9:128608872-128609284 | Rare:107; Clinvar:5; Clinvar (benign):11 | ||||
| chr9:128632214-128632548 | Common:1; Rare:98; Clinvar:1; Clinvar (benign):12 | ||||
| chr9:128656646-128656760 | Common:2; Rare:52; Clinvar (pathogenic):1 | ||||
| chr9:128683178-128683513 | Common:6; Rare:47 | ||||
| chr9:128683521-128683989 | Rare:114 |