| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124386255-124386437 | Common:1; Rare:27 | ||||
| chr9:124658427-124658443 | Rare:2 | ||||
| chr9:125153658-125153951 | Common:2; Rare:60 | ||||
| chr9:125239049-125239530 | Rare:94 | ||||
| chr9:127819621-127819711 | Rare:29; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr9:128113936-128114088 | Common:1; Rare:21 | ||||
| chr9:128115244-128115401 | Common:2; Rare:28 | ||||
| chr9:128684465-128684555 | Rare:22 | ||||
| chr9:128907069-128907256 | Common:1; Rare:40 | ||||
| chr9:129320875-129321013 | Rare:18 | ||||
| chr9:129334113-129334282 | Common:2; Rare:32 | ||||
| chr9:129488439-129488768 | Common:2; Rare:86 | ||||
| chr9:129488781-129489145 | Common:2; Rare:65 | ||||
| chr9:129490690-129490848 | Rare:28 | ||||
| chr9:129495926-129496248 | Common:2; Rare:101 |