| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18039050-18039689 | Common:5; Rare:177; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18087783-18088009 | Rare:63 | ||||
| chr17:18182980-18183134 | Rare:51 | ||||
| chr17:18183282-18183507 | Rare:57 | ||||
| chr17:18184032-18184334 | Common:1; Rare:109 | ||||
| chr17:18184724-18184908 | Common:1; Rare:41 | ||||
| chr17:18225370-18225661 | Common:3; Rare:92 | ||||
| chr17:18260413-18260678 | Rare:77 | ||||
| chr17:18314878-18315353 | Common:2; Rare:132 | ||||
| chr17:18363380-18363648 | Common:3; Rare:92 | ||||
| chr17:18682211-18682465 | Common:8; Rare:26 | ||||
| chr17:18697966-18698028 | Common:1; Rare:14 | ||||
| chr17:18721981-18722327 | Common:4; Rare:51 | ||||
| chr17:18781076-18781318 | Common:5; Rare:68 | ||||
| chr17:18856140-18856381 | Common:1; Rare:46 |