| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124940969-124941171 | Common:3; Rare:69 | ||||
| chr9:125189725-125189905 | Rare:100 | ||||
| chr9:125200440-125200590 | Common:1; Rare:57 | ||||
| chr9:125241317-125241686 | Common:3; Rare:110 | ||||
| chr9:125261775-125261841 | Rare:24 | ||||
| chr9:126804869-126805064 | Common:2; Rare:62 | ||||
| chr9:127224382-127224673 | Common:1; Rare:80 | ||||
| chr9:127245197-127245341 | Rare:35 | ||||
| chr9:127264717-127264874 | Rare:31 | ||||
| chr9:127424072-127424450 | Common:1; Rare:111 | ||||
| chr9:127451274-127451565 | Common:3; Rare:120; Clinvar (benign):1 | ||||
| chr9:127612018-127612393 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:127877656-127877771 | Rare:24 | ||||
| chr9:127899555-127899728 | Rare:63 | ||||
| chr9:127930801-127930934 | Common:1; Rare:28 |