| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26892299-26892574 | Common:1; Rare:136 | ||||
| chr9:26892632-26892918 | Common:2; Rare:132 | ||||
| chr9:26947107-26947281 | Common:1; Rare:67 | ||||
| chr9:26947383-26947497 | Rare:41 | ||||
| chr9:27573426-27573548 | Common:5; Rare:75 | ||||
| chr9:32526178-32526389 | Common:3; Rare:64 | ||||
| chr9:32552541-32552829 | Common:2; Rare:68; Clinvar:2 | ||||
| chr9:32572937-32572998 | Rare:22 | ||||
| chr9:32573011-32573226 | Common:3; Rare:73 | ||||
| chr9:33001562-33001774 | Common:3; Rare:99; Clinvar (benign):3 | ||||
| chr9:33025093-33025380 | Common:6; Rare:119 | ||||
| chr9:33076604-33076844 | Common:2; Rare:82 | ||||
| chr9:33167292-33167575 | Rare:107; Clinvar:1 | ||||
| chr9:33264676-33265150 | Common:1; Rare:135 | ||||
| chr9:33277412-33277699 | Common:1; Rare:45 |