| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128504601-128504791 | Rare:89; Clinvar:5 | ||||
| chr9:128552398-128552622 | Rare:88; Clinvar:1 | ||||
| chr9:128656635-128656816 | Common:2; Rare:83; Clinvar (pathogenic):1 | ||||
| chr9:128724089-128724472 | Common:3; Rare:125 | ||||
| chr9:128771871-128772051 | Common:1; Rare:51 | ||||
| chr9:128787143-128787341 | Common:3; Rare:68 | ||||
| chr9:128881929-128882206 | Common:2; Rare:95 | ||||
| chr9:128947549-128947735 | Common:1; Rare:89; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:129110671-129110953 | Common:3; Rare:64 | ||||
| chr9:129141878-129142058 | Common:4; Rare:39 | ||||
| chr9:129835210-129835486 | Common:2; Rare:113 | ||||
| chr9:130043097-130043292 | Common:2; Rare:61 | ||||
| chr9:130053854-130053978 | Common:1; Rare:52 | ||||
| chr9:130579410-130579671 | Common:4; Rare:99 | ||||
| chr9:130693544-130693845 | Common:1; Rare:105 |