| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96778040-96778169 | Rare:39 | ||||
| chr9:97501480-97501798 | Common:6; Rare:79 | ||||
| chr9:97633267-97633700 | Common:4; Rare:127 | ||||
| chr9:97633709-97633861 | Common:2; Rare:50 | ||||
| chr9:97922471-97922580 | Common:3; Rare:55 | ||||
| chr9:97983153-97983596 | Common:2; Rare:167 | ||||
| chr9:97984225-97984590 | Common:1; Rare:153 | ||||
| chr9:98056565-98056776 | Common:1; Rare:71 | ||||
| chr9:98255593-98255862 | Common:3; Rare:81 | ||||
| chr9:98943541-98943993 | Common:5; Rare:132 | ||||
| chr9:99221906-99222341 | Common:2; Rare:167; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99821682-99822006 | Rare:93 | ||||
| chr9:99906562-99906694 | Rare:64 | ||||
| chr9:100098951-100099332 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352831-100353092 | Rare:96 |