| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26892130-26892650 | Common:7; Rare:349 | ||||
| chr9:26892717-26892895 | Common:2; Rare:164 | ||||
| chr9:26947105-26947660 | Common:4; Rare:298 | ||||
| chr9:26956243-26956470 | Common:4; Rare:162 | ||||
| chr9:27573444-27573551 | Common:5; Rare:67 | ||||
| chr9:32384444-32384728 | Common:2; Rare:189 | ||||
| chr9:32526164-32526389 | Common:4; Rare:74 | ||||
| chr9:32552516-32552644 | Common:2; Rare:47; Clinvar:4 | ||||
| chr9:32573051-32573218 | Common:4; Rare:120 | ||||
| chr9:33001501-33001835 | Common:6; Rare:264; Clinvar (benign):8 | ||||
| chr9:33025015-33025370 | Common:14; Rare:276 | ||||
| chr9:33076610-33076854 | Common:4; Rare:161 | ||||
| chr9:33167133-33167590 | Common:2; Rare:287; Clinvar:9 | ||||
| chr9:33264596-33265072 | Common:2; Rare:266 | ||||
| chr9:33290343-33290591 | Common:4; Rare:177 |