| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17836809-17836902 | Common:1; Rare:26 | ||||
| chr17:18039073-18039416 | Common:3; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18183188-18183487 | Rare:73 | ||||
| chr17:18183799-18183931 | Rare:55 | ||||
| chr17:18184557-18184612 | Rare:16 | ||||
| chr17:18184736-18184900 | Common:1; Rare:37 | ||||
| chr17:18246394-18246696 | Common:3; Rare:101 | ||||
| chr17:18247028-18247441 | Common:8; Rare:202 | ||||
| chr17:18254531-18254823 | Rare:101 | ||||
| chr17:18260440-18260668 | Rare:67 | ||||
| chr17:18314898-18315339 | Common:1; Rare:126 | ||||
| chr17:18781091-18781305 | Common:5; Rare:59 | ||||
| chr17:18856195-18856362 | Common:1; Rare:27 | ||||
| chr17:19004724-19004882 | Common:1; Rare:53 | ||||
| chr17:19377882-19378033 | Common:1; Rare:38 |