| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33025041-33025864 | Common:13; Rare:329 | ||||
| chr9:33076587-33076753 | Common:2; Rare:60 | ||||
| chr9:33167079-33167534 | Common:1; Rare:161; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:33167763-33167908 | Rare:29 | ||||
| chr9:33260433-33260598 | Rare:31 | ||||
| chr9:33264590-33264916 | Common:1; Rare:91 | ||||
| chr9:33264937-33265147 | Rare:65 | ||||
| chr9:33290347-33290570 | Common:2; Rare:84 | ||||
| chr9:33393819-33393918 | Rare:25 | ||||
| chr9:33402608-33402766 | Rare:33 | ||||
| chr9:33473826-33474149 | Common:4; Rare:99 | ||||
| chr9:33524225-33524461 | Common:4; Rare:61 | ||||
| chr9:33817634-33817718 | Rare:25 | ||||
| chr9:34048844-34049014 | Common:2; Rare:75 | ||||
| chr9:34049132-34049308 | Common:1; Rare:47 |