| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47695522-47695725 | Common:1; Rare:47 | ||||
| chr17:47733033-47733276 | Common:1; Rare:55 | ||||
| chr17:47821712-47821944 | Common:2; Rare:53 | ||||
| chr17:47831455-47831676 | Rare:73 | ||||
| chr17:47841120-47841471 | Rare:77 | ||||
| chr17:47896207-47896316 | Common:1; Rare:36 | ||||
| chr17:47896431-47896581 | Rare:31 | ||||
| chr17:47941316-47941760 | Rare:118; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47941777-47941797 | Rare:4; Clinvar:1 | ||||
| chr17:47970717-47971185 | Common:4; Rare:118 | ||||
| chr17:47971238-47971406 | Rare:55 | ||||
| chr17:48037778-48037876 | Common:1; Rare:25 | ||||
| chr17:48047586-48048455 | Common:5; Rare:242 | ||||
| chr17:48048581-48048835 | Common:4; Rare:48 | ||||
| chr17:48049086-48049160 | Common:2; Rare:16 |