| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133336121-133336359 | Common:1; Rare:101 | ||||
| chr9:133348030-133348258 | Common:3; Rare:90 | ||||
| chr9:133356443-133356618 | Common:1; Rare:82; Clinvar (benign):2 | ||||
| chr9:133375999-133376384 | Common:2; Rare:141 | ||||
| chr9:133417939-133418312 | Common:4; Rare:91 | ||||
| chr9:134135354-134135403 | Rare:10 | ||||
| chr9:134641551-134641822 | Common:2; Rare:83; Clinvar (benign):1 | ||||
| chr9:135499856-135499970 | Common:3; Rare:31 | ||||
| chr9:135882765-135882856 | Common:1; Rare:27 | ||||
| chr9:136118817-136119017 | Common:4; Rare:88 | ||||
| chr9:136410610-136410686 | Rare:39 | ||||
| chr9:136745824-136746172 | Common:1; Rare:100 | ||||
| chr9:136849554-136849760 | Common:1; Rare:82 | ||||
| chr9:136886249-136886528 | Common:2; Rare:81 |