| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125240711-125241150 | Rare:118 | ||||
| chr9:125241256-125241673 | Common:2; Rare:123 | ||||
| chr9:125261702-125261848 | Common:1; Rare:55 | ||||
| chr9:125707176-125707319 | Common:2; Rare:47 | ||||
| chr9:127451365-127451523 | Common:2; Rare:56 | ||||
| chr9:127854483-127854731 | Rare:63; Clinvar:7; Clinvar (benign):1 | ||||
| chr9:128091260-128091459 | Rare:39 | ||||
| chr9:128191507-128191847 | Common:2; Rare:87 | ||||
| chr9:128275904-128276302 | Common:5; Rare:175 | ||||
| chr9:128322417-128322624 | Common:1; Rare:56 | ||||
| chr9:128552414-128552597 | Rare:72; Clinvar:1 | ||||
| chr9:128656634-128656803 | Common:2; Rare:78; Clinvar (pathogenic):1 | ||||
| chr9:128683521-128683901 | Rare:82 | ||||
| chr9:128692697-128692980 | Rare:55 | ||||
| chr9:128724086-128724451 | Common:1; Rare:120 |