| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122940854-122941062 | Common:2; Rare:84 | ||||
| chr9:124861908-124862145 | Common:1; Rare:103 | ||||
| chr9:124940969-124941171 | Common:3; Rare:69 | ||||
| chr9:125189725-125190019 | Common:1; Rare:135 | ||||
| chr9:125200462-125200590 | Rare:48 | ||||
| chr9:125241288-125241686 | Common:3; Rare:122 | ||||
| chr9:126804874-126805070 | Common:3; Rare:62 | ||||
| chr9:127122496-127123034 | Common:4; Rare:144 | ||||
| chr9:127224364-127224654 | Rare:76 | ||||
| chr9:127397050-127397201 | Common:2; Rare:50 | ||||
| chr9:127424253-127424440 | Common:1; Rare:61 | ||||
| chr9:127451263-127451557 | Common:3; Rare:123; Clinvar (benign):1 | ||||
| chr9:127612009-127612318 | Common:1; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127899549-127899752 | Common:1; Rare:74 | ||||
| chr9:128149287-128149457 | Rare:32 |