| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:75088177-75088563 | Common:3; Rare:140 | ||||
| chr9:83707926-83708011 | Rare:34 | ||||
| chr9:83980530-83980783 | Common:3; Rare:103 | ||||
| chr9:86354390-86354629 | Common:1; Rare:102 | ||||
| chr9:89310910-89311205 | Common:2; Rare:86 | ||||
| chr9:92293672-92293907 | Common:4; Rare:80 | ||||
| chr9:92325329-92325643 | Common:5; Rare:73 | ||||
| chr9:97633484-97633826 | Common:4; Rare:111 | ||||
| chr9:101398570-101398887 | Common:1; Rare:110 | ||||
| chr9:110256485-110256720 | Common:3; Rare:80 | ||||
| chr9:112379800-112380142 | Common:3; Rare:140 | ||||
| chr9:113221286-113221598 | Rare:96 | ||||
| chr9:113275397-113275689 | Common:4; Rare:84; Clinvar (pathogenic):1 | ||||
| chr9:120793381-120793526 | Rare:50 | ||||
| chr9:121268025-121268198 | Common:1; Rare:63 |