| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:145052193-145052518 | Common:10; Rare:95 | ||||
| chr9:214561-215205 | Common:12; Rare:367; Clinvar:6; Clinvar (benign):6 | ||||
| chr9:2015054-2015387 | Common:3; Rare:99 | ||||
| chr9:2017476-2017724 | Rare:77 | ||||
| chr9:2844043-2844359 | Common:5; Rare:124 | ||||
| chr9:3526384-3526512 | Common:4; Rare:66 | ||||
| chr9:4490074-4490249 | Common:2; Rare:46 | ||||
| chr9:4490354-4490676 | Common:1; Rare:110; Clinvar:5 | ||||
| chr9:4662017-4662348 | Common:5; Rare:115 | ||||
| chr9:4666309-4666603 | Common:3; Rare:73 | ||||
| chr9:4679423-4679791 | Common:1; Rare:161 | ||||
| chr9:4984741-4985090 | Common:1; Rare:128 | ||||
| chr9:5437813-5438071 | Common:2; Rare:84 | ||||
| chr9:6015584-6015700 | Rare:52 | ||||
| chr9:6645692-6645911 | Rare:71 |