| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128787076-128787348 | Common:4; Rare:87 | ||||
| chr9:128881925-128882189 | Common:1; Rare:90 | ||||
| chr9:128947601-128947738 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129111194-129111421 | Common:2; Rare:74 | ||||
| chr9:129626004-129626200 | Common:3; Rare:50 | ||||
| chr9:129835126-129835502 | Common:4; Rare:144 | ||||
| chr9:130042954-130042975 | Rare:3 | ||||
| chr9:130042980-130043452 | Common:3; Rare:143 | ||||
| chr9:130053864-130053933 | Common:1; Rare:22 | ||||
| chr9:131125446-131125651 | Common:1; Rare:99 | ||||
| chr9:131270533-131270806 | Common:4; Rare:56 | ||||
| chr9:131275926-131276133 | Rare:57 | ||||
| chr9:131276438-131276635 | Common:2; Rare:41 | ||||
| chr9:132354922-132355339 | Common:5; Rare:139 | ||||
| chr9:132670390-132670524 | Rare:47 |