| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128191732-128191858 | Common:1; Rare:30 | ||||
| chr9:128261502-128261752 | Rare:77 | ||||
| chr9:128275897-128276316 | Common:5; Rare:186 | ||||
| chr9:128322187-128322624 | Common:2; Rare:152 | ||||
| chr9:128322731-128322890 | Common:2; Rare:73; Clinvar (benign):5 | ||||
| chr9:128371216-128371418 | Rare:79 | ||||
| chr9:128422939-128423252 | Common:2; Rare:80 | ||||
| chr9:128455802-128456243 | Common:2; Rare:132 | ||||
| chr9:128552395-128552694 | Rare:113; Clinvar:6; Clinvar (benign):3 | ||||
| chr9:128656542-128657021 | Common:2; Rare:171; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:128689426-128690000 | Rare:213 | ||||
| chr9:128692640-128692686 | Common:1; Rare:11 | ||||
| chr9:128692693-128692981 | Rare:55 | ||||
| chr9:128724001-128724467 | Common:2; Rare:175 | ||||
| chr9:128771838-128772005 | Rare:47 |