| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2303716-2303987 | Common:2; Rare:103 | ||||
| chr17:2336433-2336563 | Rare:47 | ||||
| chr17:2511812-2511935 | Common:2; Rare:35 | ||||
| chr17:2593464-2593664 | Common:2; Rare:77 | ||||
| chr17:2593861-2593993 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:2776547-2776896 | Common:5; Rare:104 | ||||
| chr17:3668532-3668844 | Common:3; Rare:127 | ||||
| chr17:3723767-3723907 | Common:1; Rare:80 | ||||
| chr17:4143011-4143244 | Rare:76 | ||||
| chr17:4143607-4143750 | Common:4; Rare:85 | ||||
| chr17:4263937-4264096 | Rare:64 | ||||
| chr17:4366626-4366791 | Common:1; Rare:66 | ||||
| chr17:4555331-4555503 | Common:3; Rare:78 | ||||
| chr17:4704117-4704260 | Rare:75 | ||||
| chr17:4731304-4731481 | Common:2; Rare:51 |