| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26892738-26892847 | Rare:60 | ||||
| chr9:26947107-26947268 | Common:1; Rare:60 | ||||
| chr9:32573064-32573190 | Common:2; Rare:50 | ||||
| chr9:33001538-33001751 | Common:3; Rare:106; Clinvar (benign):4 | ||||
| chr9:33025071-33025374 | Common:7; Rare:124 | ||||
| chr9:33290370-33290563 | Common:2; Rare:73 | ||||
| chr9:34126630-34126843 | Common:1; Rare:63 | ||||
| chr9:34178933-34179058 | Common:1; Rare:33 | ||||
| chr9:34329228-34329606 | Rare:114 | ||||
| chr9:34646510-34646696 | Common:1; Rare:54; Clinvar:2 | ||||
| chr9:35080022-35080153 | Common:2; Rare:34; Clinvar (benign):1 | ||||
| chr9:35657857-35658318 | Common:7; Rare:402; Clinvar:41; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35732119-35732326 | Common:1; Rare:54 | ||||
| chr9:35732443-35732631 | Common:1; Rare:48 | ||||
| chr9:35748978-35749347 | Common:2; Rare:137 |