| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122905281-122905552 | Common:2; Rare:108 | ||||
| chr9:122913268-122913415 | Common:2; Rare:30 | ||||
| chr9:122931490-122931710 | Common:3; Rare:48 | ||||
| chr9:122940781-122941050 | Common:2; Rare:105 | ||||
| chr9:124415365-124415529 | Common:1; Rare:73 | ||||
| chr9:124861903-124862136 | Common:1; Rare:96 | ||||
| chr9:124940969-124941156 | Common:3; Rare:62 | ||||
| chr9:125189725-125189869 | Rare:87 | ||||
| chr9:125200440-125200599 | Common:1; Rare:62 | ||||
| chr9:125241157-125241703 | Common:5; Rare:173 | ||||
| chr9:125261632-125261848 | Common:2; Rare:77 | ||||
| chr9:126804912-126805070 | Common:3; Rare:54 | ||||
| chr9:127424106-127424450 | Common:1; Rare:96 | ||||
| chr9:127451274-127451562 | Common:3; Rare:119; Clinvar (benign):1 | ||||
| chr9:127579008-127579306 | Common:4; Rare:60 |