| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127937824-127937932 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128091338-128091472 | Rare:27 | ||||
| chr9:128160046-128160455 | Common:2; Rare:100 | ||||
| chr9:128191335-128191651 | Rare:90 | ||||
| chr9:128191750-128191826 | Common:1; Rare:19 | ||||
| chr9:128275936-128276279 | Common:4; Rare:157 | ||||
| chr9:128322410-128322634 | Common:1; Rare:62 | ||||
| chr9:128322751-128322884 | Common:2; Rare:64; Clinvar (benign):5 | ||||
| chr9:128340419-128340695 | Common:2; Rare:87 | ||||
| chr9:128371199-128371392 | Rare:68 | ||||
| chr9:128504641-128504798 | Rare:72; Clinvar:5 | ||||
| chr9:128552398-128552611 | Rare:81; Clinvar:1 | ||||
| chr9:128656656-128657002 | Common:2; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:128689407-128689615 | Rare:77 | ||||
| chr9:128724097-128724338 | Common:1; Rare:72 |