| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26956275-26956464 | Common:2; Rare:74 | ||||
| chr9:27573422-27573553 | Common:5; Rare:79 | ||||
| chr9:32384432-32384732 | Common:1; Rare:104 | ||||
| chr9:32526184-32526370 | Common:3; Rare:46 | ||||
| chr9:32573068-32573270 | Common:4; Rare:77 | ||||
| chr9:33025071-33025414 | Common:7; Rare:136 | ||||
| chr9:33076591-33076865 | Common:2; Rare:89 | ||||
| chr9:33166761-33166987 | Rare:75; Clinvar:3 | ||||
| chr9:33167038-33167578 | Common:1; Rare:185; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:33264718-33265147 | Rare:119 | ||||
| chr9:33290343-33290578 | Common:2; Rare:87 | ||||
| chr9:33473823-33474143 | Common:4; Rare:99 | ||||
| chr9:34048860-34048966 | Rare:45 | ||||
| chr9:34049175-34049267 | Common:1; Rare:22 | ||||
| chr9:34126375-34126425 | Rare:19 |