| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:94259308-94259331 | Rare:7 | ||||
| chr9:94639344-94639571 | Common:1; Rare:65; Clinvar:7; Clinvar (benign):1 | ||||
| chr9:94640168-94640304 | Common:1; Rare:32 | ||||
| chr9:94640309-94640337 | Rare:6 | ||||
| chr9:94726547-94726732 | Rare:52 | ||||
| chr9:95004090-95004232 | Rare:40 | ||||
| chr9:95317663-95317846 | Common:1; Rare:58; Clinvar:2 | ||||
| chr9:95875453-95875708 | Common:1; Rare:86 | ||||
| chr9:95875961-95876056 | Common:5; Rare:48 | ||||
| chr9:96383570-96383783 | Common:3; Rare:66 | ||||
| chr9:96655284-96655424 | Rare:39 | ||||
| chr9:96778057-96778154 | Rare:30 | ||||
| chr9:97411994-97412190 | Common:3; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:97501506-97501766 | Common:6; Rare:68 | ||||
| chr9:97633267-97633466 | Common:1; Rare:54 |