| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16653797-16654056 | Rare:66 | ||||
| chr17:17281182-17281311 | Rare:60 | ||||
| chr17:17476750-17477054 | Common:4; Rare:75 | ||||
| chr17:17496393-17496553 | Rare:41 | ||||
| chr17:17591580-17591964 | Common:2; Rare:111 | ||||
| chr17:18039091-18039439 | Common:5; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18087838-18088021 | Rare:52 | ||||
| chr17:18183284-18183481 | Rare:44 | ||||
| chr17:18225352-18225661 | Common:3; Rare:98 | ||||
| chr17:18254577-18254823 | Rare:85 | ||||
| chr17:18260413-18260720 | Rare:94 | ||||
| chr17:18314921-18315348 | Common:1; Rare:123 | ||||
| chr17:18363414-18363705 | Common:5; Rare:96 | ||||
| chr17:18682206-18682479 | Common:9; Rare:27 | ||||
| chr17:18697966-18698043 | Common:1; Rare:18 |