| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:23826298-23826482 | Common:1; Rare:77 | ||||
| chr9:26892338-26892505 | Rare:75 | ||||
| chr9:26892726-26892895 | Common:1; Rare:79 | ||||
| chr9:26947107-26947300 | Common:1; Rare:69 | ||||
| chr9:26947444-26947566 | Common:1; Rare:33 | ||||
| chr9:26956246-26956497 | Common:2; Rare:94 | ||||
| chr9:26976376-26976677 | Rare:56 | ||||
| chr9:27573422-27573560 | Common:5; Rare:82 | ||||
| chr9:27573716-27573972 | Common:2; Rare:82; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384479-32384732 | Common:1; Rare:92 | ||||
| chr9:32526176-32526253 | Common:1; Rare:33 | ||||
| chr9:32551995-32552372 | Common:2; Rare:103 | ||||
| chr9:32552541-32552695 | Common:1; Rare:28; Clinvar:2 | ||||
| chr9:32573005-32573416 | Common:4; Rare:119 | ||||
| chr9:33001537-33001769 | Common:3; Rare:114; Clinvar (benign):4 |