| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127122633-127122868 | Common:3; Rare:60 | ||||
| chr9:127451279-127451533 | Common:2; Rare:111 | ||||
| chr9:127877667-127877767 | Rare:18 | ||||
| chr9:127916989-127917336 | Common:1; Rare:103 | ||||
| chr9:128160056-128160383 | Common:2; Rare:82 | ||||
| chr9:128275919-128276302 | Common:5; Rare:172 | ||||
| chr9:128322410-128322508 | Common:1; Rare:34 | ||||
| chr9:128322713-128322896 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:128371203-128371395 | Rare:71 | ||||
| chr9:128552383-128552611 | Rare:84; Clinvar:1 | ||||
| chr9:128656662-128656816 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
| chr9:128689516-128689585 | Rare:38 | ||||
| chr9:128724095-128724464 | Common:2; Rare:121 | ||||
| chr9:128787103-128787345 | Common:4; Rare:80 | ||||
| chr9:128881916-128882206 | Common:2; Rare:97 |