| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:145002827-145002925 | Common:1; Rare:33 | ||||
| chr9:16726835-16726934 | Common:1; Rare:21 | ||||
| chr9:21559832-21559973 | Common:1; Rare:79 | ||||
| chr9:35657707-35657764 | Common:1; Rare:30; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35724065-35724227 | Rare:43 | ||||
| chr9:37079790-37079994 | Common:4; Rare:68 | ||||
| chr9:37466549-37466642 | Common:1; Rare:21 | ||||
| chr9:40992025-40992410 | Common:7; Rare:27 | ||||
| chr9:41358764-41358904 | Common:1; Rare:45 | ||||
| chr9:62802116-62802177 | |||||
| chr9:62802665-62802780 | |||||
| chr9:70413407-70413637 | Rare:71 | ||||
| chr9:70418966-70419195 | Common:2; Rare:56 | ||||
| chr9:70479946-70480153 | Rare:35 | ||||
| chr9:87148487-87148559 | Rare:17 |