| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17496388-17496516 | Rare:31 | ||||
| chr17:17591595-17591932 | Common:1; Rare:96 | ||||
| chr17:17823573-17823837 | Common:5; Rare:124 | ||||
| chr17:18039152-18039365 | Common:3; Rare:53; Clinvar (benign):1 | ||||
| chr17:18183282-18183507 | Rare:57 | ||||
| chr17:18183713-18183931 | Rare:101 | ||||
| chr17:18184736-18185008 | Common:1; Rare:59 | ||||
| chr17:18253360-18253661 | Rare:107 | ||||
| chr17:18254520-18254824 | Rare:104 | ||||
| chr17:18314921-18315317 | Common:1; Rare:110 | ||||
| chr17:18781091-18781305 | Common:5; Rare:59 | ||||
| chr17:18856168-18856372 | Common:1; Rare:38 | ||||
| chr17:19362570-19362773 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19377892-19378033 | Common:1; Rare:35 | ||||
| chr17:19378160-19378554 | Common:2; Rare:94 |