| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125200421-125200590 | Common:1; Rare:64 | ||||
| chr9:125241270-125241708 | Common:4; Rare:139 | ||||
| chr9:125261657-125261848 | Common:2; Rare:71 | ||||
| chr9:125650421-125650693 | Rare:47 | ||||
| chr9:125707131-125707426 | Common:3; Rare:102 | ||||
| chr9:127122718-127123015 | Common:3; Rare:88 | ||||
| chr9:127245158-127245351 | Common:1; Rare:45 | ||||
| chr9:127424216-127424440 | Common:1; Rare:69 | ||||
| chr9:127449614-127449787 | Rare:42 | ||||
| chr9:127450735-127450874 | Common:2; Rare:35 | ||||
| chr9:127451274-127451557 | Common:3; Rare:118; Clinvar (benign):1 | ||||
| chr9:127579018-127579305 | Common:4; Rare:59 | ||||
| chr9:127612018-127612323 | Common:1; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127937807-127937923 | Common:1; Rare:36; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:128098289-128098549 | Common:1; Rare:56 |