| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122931473-122931666 | Common:3; Rare:35 | ||||
| chr9:123929928-123930247 | Rare:96 | ||||
| chr9:124011325-124011609 | Common:1; Rare:56 | ||||
| chr9:124861908-124862134 | Common:1; Rare:95 | ||||
| chr9:124940969-124941156 | Common:3; Rare:62 | ||||
| chr9:125189733-125190015 | Common:1; Rare:133 | ||||
| chr9:125200440-125200561 | Common:1; Rare:40 | ||||
| chr9:125241294-125241657 | Common:2; Rare:110 | ||||
| chr9:125261730-125261848 | Common:1; Rare:41 | ||||
| chr9:125707192-125707319 | Common:2; Rare:41 | ||||
| chr9:126804876-126805095 | Common:3; Rare:77 | ||||
| chr9:127264822-127264874 | Rare:10 | ||||
| chr9:127424106-127424440 | Common:1; Rare:92 | ||||
| chr9:127451268-127451580 | Common:3; Rare:124; Clinvar (benign):1 | ||||
| chr9:127612017-127612379 | Common:2; Rare:130; Clinvar:4; Clinvar (benign):3 |