| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133131112-133131186 | Rare:12 | ||||
| chr9:133163883-133164022 | Common:3; Rare:36 | ||||
| chr9:133336121-133336418 | Common:2; Rare:131 | ||||
| chr9:133348029-133348276 | Common:3; Rare:103 | ||||
| chr9:133348772-133349042 | Common:1; Rare:101 | ||||
| chr9:133356440-133356616 | Common:1; Rare:83; Clinvar (benign):2 | ||||
| chr9:133375959-133376366 | Common:3; Rare:146 | ||||
| chr9:133417901-133418300 | Common:5; Rare:98 | ||||
| chr9:134641547-134641841 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:135499847-135499970 | Common:3; Rare:35 | ||||
| chr9:136118774-136119017 | Common:4; Rare:100 | ||||
| chr9:136373634-136373732 | Rare:15; Clinvar:2 | ||||
| chr9:136410610-136410680 | Rare:35 | ||||
| chr9:136662600-136662972 | Common:2; Rare:90 | ||||
| chr9:136745826-136746176 | Common:1; Rare:99 |