| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128275891-128276302 | Common:5; Rare:176 | ||||
| chr9:128322409-128322570 | Common:1; Rare:52 | ||||
| chr9:128322739-128322896 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:128340456-128340691 | Common:2; Rare:78 | ||||
| chr9:128371235-128371404 | Rare:63 | ||||
| chr9:128504628-128504782 | Rare:67; Clinvar:5 | ||||
| chr9:128552394-128552611 | Rare:81; Clinvar:1 | ||||
| chr9:128656656-128656785 | Common:2; Rare:62; Clinvar (pathogenic):1 | ||||
| chr9:128724081-128724467 | Common:2; Rare:128 | ||||
| chr9:128787071-128787341 | Common:4; Rare:86 | ||||
| chr9:128881907-128882206 | Common:2; Rare:100 | ||||
| chr9:128922000-128922324 | Common:1; Rare:78 | ||||
| chr9:128947555-128947725 | Common:1; Rare:82; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129110639-129111029 | Common:5; Rare:121 | ||||
| chr9:129111316-129111603 | Common:2; Rare:75 |