| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92535978-92536217 | Common:1; Rare:30 | ||||
| chr9:92670017-92670386 | Common:1; Rare:114 | ||||
| chr9:93451472-93451699 | Common:3; Rare:67 | ||||
| chr9:93452881-93453014 | Common:1; Rare:30 | ||||
| chr9:93453520-93453699 | Rare:42 | ||||
| chr9:95004090-95004232 | Rare:40 | ||||
| chr9:95875453-95875703 | Common:1; Rare:82 | ||||
| chr9:95875958-95876059 | Common:6; Rare:51; Clinvar (pathogenic):1 | ||||
| chr9:96383509-96383777 | Common:3; Rare:89 | ||||
| chr9:96655289-96655397 | Rare:29 | ||||
| chr9:96778054-96778156 | Rare:33 | ||||
| chr9:97501506-97501802 | Common:6; Rare:75 | ||||
| chr9:97633271-97633848 | Common:6; Rare:177 | ||||
| chr9:97922471-97922585 | Common:3; Rare:56 | ||||
| chr9:98119186-98119518 | Common:2; Rare:73 |