| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:32573068-32573218 | Common:2; Rare:57 | ||||
| chr9:33025068-33025312 | Common:6; Rare:102 | ||||
| chr9:34329213-34329598 | Rare:119 | ||||
| chr9:35658003-35658322 | Common:5; Rare:240; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):33 | ||||
| chr9:35673842-35673962 | Common:2; Rare:35 | ||||
| chr9:35732089-35732320 | Rare:66 | ||||
| chr9:35732373-35732683 | Common:3; Rare:78 | ||||
| chr9:36258438-36258607 | Common:2; Rare:38; Clinvar:1 | ||||
| chr9:70258834-70258993 | Common:3; Rare:67 | ||||
| chr9:75088140-75088570 | Common:3; Rare:153 | ||||
| chr9:76459049-76459234 | Common:1; Rare:63 | ||||
| chr9:83980566-83980844 | Common:5; Rare:118 | ||||
| chr9:86354388-86354636 | Common:1; Rare:108 | ||||
| chr9:88388233-88388481 | Common:1; Rare:104 | ||||
| chr9:97633535-97633832 | Common:4; Rare:92 |