| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133418008-133418339 | Common:4; Rare:73 | ||||
| chr9:133459820-133460051 | Common:1; Rare:94 | ||||
| chr9:133479048-133479390 | Common:1; Rare:101 | ||||
| chr9:133534449-133534849 | Rare:168 | ||||
| chr9:133738080-133738570 | Common:6; Rare:108 | ||||
| chr9:133992319-133992486 | Rare:55 | ||||
| chr9:133992620-133993010 | Common:1; Rare:127 | ||||
| chr9:134067550-134067890 | Common:1; Rare:130 | ||||
| chr9:134067958-134068247 | Rare:79 | ||||
| chr9:134135271-134135444 | Common:2; Rare:29 | ||||
| chr9:134135665-134135766 | Common:2; Rare:24 | ||||
| chr9:134135850-134136200 | Common:6; Rare:111 | ||||
| chr9:134325967-134326190 | Rare:79 | ||||
| chr9:134326335-134326484 | Rare:46 | ||||
| chr9:134641537-134641822 | Common:2; Rare:86; Clinvar (benign):1 |