| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127877667-127877767 | Rare:18 | ||||
| chr9:127916999-127917261 | Rare:77 | ||||
| chr9:127937816-127937878 | Common:1; Rare:24; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:128067310-128067589 | Common:3; Rare:60 | ||||
| chr9:128098289-128098552 | Common:1; Rare:57 | ||||
| chr9:128149240-128149520 | Rare:60 | ||||
| chr9:128160008-128160455 | Common:2; Rare:106 | ||||
| chr9:128191515-128191642 | Rare:34 | ||||
| chr9:128191753-128191938 | Common:1; Rare:50 | ||||
| chr9:128275919-128276312 | Common:5; Rare:177 | ||||
| chr9:128322406-128322621 | Common:1; Rare:63 | ||||
| chr9:128322711-128322866 | Common:2; Rare:58; Clinvar (benign):5 | ||||
| chr9:128371235-128371428 | Rare:75 | ||||
| chr9:128552408-128552611 | Rare:79; Clinvar:1 | ||||
| chr9:128656662-128656988 | Common:1; Rare:109; Clinvar (pathogenic):1 |