| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:714785-714899 | Common:2; Rare:40 | ||||
| chr17:752152-752318 | Common:2; Rare:68 | ||||
| chr17:979733-979996 | Common:3; Rare:124 | ||||
| chr17:1468442-1468770 | Common:7; Rare:83; Clinvar (benign):1 | ||||
| chr17:1516562-1516971 | Common:2; Rare:147 | ||||
| chr17:1648886-1649195 | Common:2; Rare:99 | ||||
| chr17:1761956-1762110 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:1829786-1830038 | Common:6; Rare:108 | ||||
| chr17:2303504-2303616 | Rare:42 | ||||
| chr17:2303716-2303987 | Common:2; Rare:103 | ||||
| chr17:2336423-2336553 | Rare:50 | ||||
| chr17:2337366-2337637 | Common:1; Rare:80 | ||||
| chr17:2511806-2511935 | Common:2; Rare:38 | ||||
| chr17:2593459-2593683 | Common:3; Rare:85; Clinvar (benign):2 | ||||
| chr17:2593851-2593987 | Common:1; Rare:39; Clinvar:3; Clinvar (benign):3 |