| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18039588-18039673 | Rare:29 | ||||
| chr17:18087845-18088018 | Rare:51 | ||||
| chr17:18183692-18183847 | Rare:69 | ||||
| chr17:18260437-18260662 | Rare:65 | ||||
| chr17:18314898-18315339 | Common:1; Rare:126 | ||||
| chr17:18682206-18682482 | Common:9; Rare:27 | ||||
| chr17:18781091-18781305 | Common:5; Rare:59 | ||||
| chr17:18856195-18856401 | Common:1; Rare:38 | ||||
| chr17:18857955-18858221 | Common:6; Rare:69 | ||||
| chr17:19362565-19362786 | Common:2; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19378162-19378530 | Common:2; Rare:90 | ||||
| chr17:19411045-19411245 | Rare:51 | ||||
| chr17:19533628-19533916 | Common:3; Rare:68 | ||||
| chr17:19648602-19648810 | Common:2; Rare:70 | ||||
| chr17:19977807-19977974 | Common:1; Rare:57 |