| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128322410-128322535 | Common:1; Rare:43 | ||||
| chr9:128322729-128322875 | Common:2; Rare:61; Clinvar (benign):5 | ||||
| chr9:128371128-128371392 | Common:1; Rare:86 | ||||
| chr9:128455992-128456169 | Common:1; Rare:57 | ||||
| chr9:128504611-128504817 | Rare:94; Clinvar:6 | ||||
| chr9:128552404-128552611 | Rare:81; Clinvar:1 | ||||
| chr9:128656644-128656840 | Common:2; Rare:83; Clinvar (pathogenic):1 | ||||
| chr9:128724064-128724472 | Common:3; Rare:140 | ||||
| chr9:128771901-128771960 | Rare:8 | ||||
| chr9:128772450-128772487 | Rare:3 | ||||
| chr9:128787155-128787341 | Common:3; Rare:64 | ||||
| chr9:128881907-128882206 | Common:2; Rare:100 | ||||
| chr9:128922004-128922314 | Common:1; Rare:72 | ||||
| chr9:128947573-128947747 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:129036341-129036672 | Common:2; Rare:90 |