| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122931490-122931662 | Common:3; Rare:30 | ||||
| chr9:124861908-124862125 | Rare:93 | ||||
| chr9:124940969-124941158 | Common:3; Rare:63 | ||||
| chr9:125189741-125189940 | Common:1; Rare:106 | ||||
| chr9:125241366-125241686 | Common:2; Rare:86 | ||||
| chr9:125261716-125261841 | Common:1; Rare:46 | ||||
| chr9:127122567-127122787 | Common:2; Rare:54 | ||||
| chr9:127451286-127451533 | Common:2; Rare:109 | ||||
| chr9:127612047-127612318 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127661434-127661699 | Common:1; Rare:54 | ||||
| chr9:128275936-128276288 | Common:4; Rare:163 | ||||
| chr9:128322410-128322485 | Rare:30 | ||||
| chr9:128322751-128322887 | Common:2; Rare:66; Clinvar (benign):5 | ||||
| chr9:128456127-128456165 | Rare:16 | ||||
| chr9:128504612-128504782 | Rare:76; Clinvar:5 |