| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75830442-75830621 | Common:1; Rare:68; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75855276-75855702 | Common:1; Rare:118 | ||||
| chr17:75878552-75878710 | Common:3; Rare:59 | ||||
| chr17:75949230-75949546 | Common:1; Rare:88; Clinvar:3 | ||||
| chr17:75978999-75979316 | Rare:92; Clinvar:4 | ||||
| chr17:75979387-75979490 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr17:76001528-76001793 | Common:1; Rare:63 | ||||
| chr17:76072497-76072636 | Rare:41 | ||||
| chr17:76103712-76103838 | Common:1; Rare:39 | ||||
| chr17:76501385-76501550 | Rare:60; Clinvar (benign):3 | ||||
| chr17:76726471-76726874 | Common:5; Rare:148 | ||||
| chr17:76737309-76737529 | Common:3; Rare:86 | ||||
| chr17:77287789-77287958 | Rare:20 | ||||
| chr17:77288245-77288286 | Rare:11 | ||||
| chr17:77323227-77323508 | Common:1; Rare:54 |