| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122913277-122913426 | Common:3; Rare:36 | ||||
| chr9:122931482-122931694 | Common:3; Rare:44 | ||||
| chr9:124861890-124862134 | Common:1; Rare:103 | ||||
| chr9:124940949-124941134 | Common:3; Rare:67 | ||||
| chr9:125143482-125143597 | Rare:52 | ||||
| chr9:125189650-125189846 | Rare:104 | ||||
| chr9:125189913-125190029 | Common:1; Rare:38 | ||||
| chr9:125200462-125200590 | Rare:48 | ||||
| chr9:125241282-125241656 | Common:2; Rare:112 | ||||
| chr9:125261702-125261866 | Common:2; Rare:61 | ||||
| chr9:126804676-126805128 | Common:5; Rare:128 | ||||
| chr9:127122718-127123076 | Common:3; Rare:114 | ||||
| chr9:127424081-127424460 | Common:1; Rare:110 | ||||
| chr9:127450735-127451062 | Common:3; Rare:73 | ||||
| chr9:127451274-127451557 | Common:3; Rare:118; Clinvar (benign):1 |