| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93451462-93451699 | Common:3; Rare:69 | ||||
| chr9:93453546-93453612 | Rare:16 | ||||
| chr9:93576512-93576763 | Common:3; Rare:77 | ||||
| chr9:94259291-94259343 | Rare:17 | ||||
| chr9:94726547-94726729 | Rare:51 | ||||
| chr9:95317675-95317827 | Common:1; Rare:45; Clinvar:1 | ||||
| chr9:95875453-95875708 | Common:1; Rare:86 | ||||
| chr9:95875961-95876066 | Common:5; Rare:53; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96778040-96778146 | Rare:33 | ||||
| chr9:97039106-97039282 | Rare:71 | ||||
| chr9:97633282-97633848 | Common:6; Rare:177 | ||||
| chr9:97697299-97697618 | Common:1; Rare:124; Clinvar:5 | ||||
| chr9:97922471-97922570 | Common:3; Rare:49 | ||||
| chr9:97984501-97984600 | Common:1; Rare:49 | ||||
| chr9:98119188-98119263 | Common:1; Rare:22 |