| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33001539-33001764 | Common:3; Rare:109; Clinvar (benign):4 | ||||
| chr9:33025061-33025414 | Common:7; Rare:140 | ||||
| chr9:33076594-33076865 | Common:2; Rare:89 | ||||
| chr9:33166745-33166966 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:33167083-33167563 | Common:1; Rare:173; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:33264467-33265147 | Common:2; Rare:215 | ||||
| chr9:33290350-33290571 | Common:2; Rare:83 | ||||
| chr9:33401341-33401528 | Rare:35 | ||||
| chr9:33402439-33402783 | Rare:67 | ||||
| chr9:33473845-33474144 | Common:4; Rare:93 | ||||
| chr9:33817633-33817927 | Common:1; Rare:84 | ||||
| chr9:34048844-34049004 | Common:2; Rare:70 | ||||
| chr9:34049178-34049293 | Common:1; Rare:29 | ||||
| chr9:34126375-34126786 | Rare:145 | ||||
| chr9:34178933-34179090 | Common:1; Rare:43 |