| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128656652-128657002 | Common:2; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:128683660-128683912 | Rare:65 | ||||
| chr9:128684969-128685098 | Rare:24 | ||||
| chr9:128724070-128724472 | Common:3; Rare:135 | ||||
| chr9:128771885-128772024 | Rare:28 | ||||
| chr9:128772456-128772487 | Rare:2 | ||||
| chr9:128787147-128787332 | Common:3; Rare:61 | ||||
| chr9:128881929-128882226 | Common:2; Rare:104 | ||||
| chr9:128912437-128912761 | Common:2; Rare:54 | ||||
| chr9:128947598-128947725 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110653-129110960 | Common:4; Rare:70 | ||||
| chr9:129139948-129140129 | Rare:36 | ||||
| chr9:129141497-129141682 | Common:3; Rare:57 | ||||
| chr9:129824075-129824417 | Common:4; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:129835214-129835492 | Common:2; Rare:112 |