| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33001560-33001721 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr9:33025071-33025382 | Common:7; Rare:127 | ||||
| chr9:33076613-33076877 | Common:2; Rare:90 | ||||
| chr9:33166880-33166966 | Rare:35 | ||||
| chr9:33167157-33167502 | Common:1; Rare:117; Clinvar:5 | ||||
| chr9:33264910-33265147 | Rare:76 | ||||
| chr9:33290383-33290570 | Common:2; Rare:74 | ||||
| chr9:33473881-33474143 | Common:2; Rare:75 | ||||
| chr9:34048857-34049267 | Common:2; Rare:132 | ||||
| chr9:34126548-34126786 | Rare:78 | ||||
| chr9:34178933-34179090 | Common:1; Rare:43 | ||||
| chr9:34329181-34329606 | Rare:134 | ||||
| chr9:34376860-34377089 | Rare:55 | ||||
| chr9:34458557-34458847 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:34612084-34612223 | Common:8; Rare:46 |