| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:94921252-94921325 | Rare:23 | ||||
| chr9:95004366-95004500 | Common:1; Rare:26 | ||||
| chr9:95055827-95056150 | Rare:65 | ||||
| chr9:95317642-95317799 | Common:1; Rare:52; Clinvar:2 | ||||
| chr9:95505871-95506216 | Common:2; Rare:118 | ||||
| chr9:95507401-95507572 | Rare:47 | ||||
| chr9:95875449-95875757 | Common:1; Rare:108 | ||||
| chr9:95875977-95876068 | Common:4; Rare:47; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96383476-96383756 | Common:3; Rare:93 | ||||
| chr9:96655307-96655392 | Rare:19 | ||||
| chr9:96778048-96778154 | Rare:33 | ||||
| chr9:97633261-97633912 | Common:7; Rare:195 | ||||
| chr9:97922421-97922600 | Common:4; Rare:90 | ||||
| chr9:97983510-97983596 | Rare:32 | ||||
| chr9:98056486-98056789 | Common:2; Rare:102 |