| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75784558-75784881 | Common:2; Rare:146 | ||||
| chr17:75855272-75855705 | Common:1; Rare:122 | ||||
| chr17:75878544-75878725 | Common:3; Rare:65 | ||||
| chr17:75904822-75905218 | Common:6; Rare:113 | ||||
| chr17:75940984-75941181 | Rare:66 | ||||
| chr17:75979046-75979315 | Rare:75; Clinvar:4 | ||||
| chr17:75979384-75979626 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr17:76027301-76027529 | Rare:51 | ||||
| chr17:76072480-76072664 | Rare:57 | ||||
| chr17:76103695-76103872 | Common:5; Rare:64 | ||||
| chr17:76353590-76353675 | Rare:36 | ||||
| chr17:76353839-76354238 | Common:1; Rare:123 | ||||
| chr17:76501379-76501566 | Rare:62; Clinvar (benign):3 | ||||
| chr17:76725840-76726124 | Common:1; Rare:75 | ||||
| chr17:76726454-76726977 | Common:5; Rare:201 |