| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:134135245-134135403 | Common:1; Rare:33 | ||||
| chr9:135499855-135499966 | Common:3; Rare:31 | ||||
| chr9:135699471-135699629 | Common:2; Rare:67 | ||||
| chr9:136410610-136410686 | Rare:39 | ||||
| chr9:136483737-136483880 | Rare:44 | ||||
| chr9:136745847-136746173 | Common:1; Rare:90 | ||||
| chr9:136746187-136746444 | Common:2; Rare:38 | ||||
| chr9:136800134-136800430 | Common:5; Rare:93 | ||||
| chr9:136807809-136808128 | Common:3; Rare:118 | ||||
| chr9:136849587-136849770 | Common:1; Rare:69 | ||||
| chr9:136944592-136944825 | Rare:103 | ||||
| chr9:136977286-136977692 | Common:1; Rare:86 | ||||
| chr9:136979944-136980283 | Rare:137 | ||||
| chr9:136996539-136996775 | Common:2; Rare:68 | ||||
| chr9:137086658-137087081 | Common:1; Rare:171; Clinvar:4; Clinvar (benign):1 |