| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2033560-2033792 | Common:1; Rare:62 | ||||
| chr17:2303496-2303633 | Rare:50 | ||||
| chr17:2303774-2303973 | Common:2; Rare:68 | ||||
| chr17:2336424-2336484 | Rare:22 | ||||
| chr17:2593460-2593655 | Common:2; Rare:77 | ||||
| chr17:2711762-2712043 | Common:2; Rare:79 | ||||
| chr17:3636226-3636496 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr17:3668552-3668826 | Common:2; Rare:107 | ||||
| chr17:3723776-3723913 | Common:1; Rare:74 | ||||
| chr17:4143004-4143255 | Rare:81 | ||||
| chr17:4143617-4143740 | Common:4; Rare:69 | ||||
| chr17:4263937-4264024 | Rare:38 | ||||
| chr17:4704108-4704260 | Rare:80 | ||||
| chr17:4731392-4731486 | Common:2; Rare:37 | ||||
| chr17:4806999-4807210 | Common:4; Rare:65 |