| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128322707-128322880 | Common:2; Rare:74; Clinvar (benign):5 | ||||
| chr9:128340148-128340364 | Common:4; Rare:67 | ||||
| chr9:128340416-128340592 | Common:1; Rare:59 | ||||
| chr9:128370634-128371034 | Common:5; Rare:83 | ||||
| chr9:128371120-128371445 | Common:1; Rare:116 | ||||
| chr9:128420190-128420470 | Common:1; Rare:65 | ||||
| chr9:128420713-128420867 | Common:2; Rare:50 | ||||
| chr9:128455952-128456218 | Common:1; Rare:84 | ||||
| chr9:128456800-128457070 | Common:1; Rare:69 | ||||
| chr9:128504488-128504860 | Common:2; Rare:142; Clinvar:7 | ||||
| chr9:128552287-128552607 | Common:1; Rare:110; Clinvar:1 | ||||
| chr9:128656609-128657034 | Common:2; Rare:144; Clinvar (pathogenic):1 | ||||
| chr9:128683599-128683866 | Rare:58 | ||||
| chr9:128684836-128685236 | Rare:108 | ||||
| chr9:128688925-128689301 | Rare:155 |