| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:83980164-83980363 | Rare:71 | ||||
| chr9:83980524-83980803 | Common:3; Rare:112 | ||||
| chr9:85741918-85742172 | Common:4; Rare:90 | ||||
| chr9:86354397-86354626 | Common:1; Rare:97 | ||||
| chr9:88388201-88388487 | Common:1; Rare:124 | ||||
| chr9:89310900-89311205 | Common:2; Rare:90 | ||||
| chr9:89318405-89318555 | Common:4; Rare:73 | ||||
| chr9:92293654-92293952 | Common:5; Rare:100 | ||||
| chr9:92670072-92670314 | Common:1; Rare:73 | ||||
| chr9:93451517-93451699 | Common:3; Rare:56 | ||||
| chr9:97039096-97039279 | Rare:73 | ||||
| chr9:97633324-97633799 | Common:6; Rare:144 | ||||
| chr9:97922485-97922618 | Common:3; Rare:61 | ||||
| chr9:98255641-98255828 | Common:3; Rare:58 | ||||
| chr9:99221930-99222323 | Common:2; Rare:142; Clinvar:2; Clinvar (benign):1 |