| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:77353234-77353635 | Common:3; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:77411357-77411623 | Common:6; Rare:81 | ||||
| chr9:77956605-77956907 | Common:1; Rare:62 | ||||
| chr9:79674193-79674265 | Common:1; Rare:11 | ||||
| chr9:83062085-83062172 | Rare:22 | ||||
| chr9:83219209-83219366 | Common:2; Rare:38 | ||||
| chr9:83473419-83473636 | Rare:39 | ||||
| chr9:83920680-83920771 | Rare:23 | ||||
| chr9:86027599-86028209 | Common:3; Rare:152 | ||||
| chr9:86049870-86050168 | Common:2; Rare:61 | ||||
| chr9:86056959-86057302 | Rare:54 | ||||
| chr9:86298001-86298315 | Common:2; Rare:44 | ||||
| chr9:86298353-86298579 | Rare:29 | ||||
| chr9:86301566-86301908 | Common:1; Rare:60 | ||||
| chr9:86304854-86305022 | Rare:28 |