| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122370710-122371052 | Common:2; Rare:68 | ||||
| chr9:122913293-122913631 | Common:2; Rare:77 | ||||
| chr9:122931482-122931689 | Common:3; Rare:41 | ||||
| chr9:124940957-124941178 | Common:3; Rare:81 | ||||
| chr9:125189733-125190050 | Common:1; Rare:142 | ||||
| chr9:125200287-125200590 | Common:1; Rare:102 | ||||
| chr9:125241317-125241679 | Common:3; Rare:106 | ||||
| chr9:125261716-125261866 | Common:2; Rare:53 | ||||
| chr9:126804924-126805061 | Common:1; Rare:42 | ||||
| chr9:126860589-126860693 | Common:2; Rare:34 | ||||
| chr9:127122555-127122786 | Common:2; Rare:56 | ||||
| chr9:127122788-127122948 | Common:2; Rare:43 | ||||
| chr9:127224315-127224652 | Rare:88 | ||||
| chr9:127424106-127424460 | Common:1; Rare:98 | ||||
| chr9:127451257-127451562 | Common:3; Rare:128; Clinvar (benign):1 |