| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:6645620-6645912 | Common:2; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:6757550-6757740 | Common:2; Rare:74 | ||||
| chr9:6757844-6758048 | Common:4; Rare:79 | ||||
| chr9:7799756-7799898 | Common:1; Rare:68 | ||||
| chr9:8857203-8857448 | Common:5; Rare:75 | ||||
| chr9:8857821-8858085 | Common:4; Rare:85 | ||||
| chr9:12775019-12775724 | Common:5; Rare:272 | ||||
| chr9:12776127-12776227 | Rare:34 | ||||
| chr9:13140025-13140146 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr9:13279090-13279490 | Common:11; Rare:135 | ||||
| chr9:13279510-13279860 | Common:4; Rare:107 | ||||
| chr9:14313984-14314659 | Common:4; Rare:297 | ||||
| chr9:14322390-14322860 | Common:3; Rare:173 | ||||
| chr9:14692691-14693013 | Common:3; Rare:107 | ||||
| chr9:14910228-14910851 | Common:2; Rare:184; Clinvar:1 |