| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3636241-3636479 | Common:4; Rare:63; Clinvar (benign):1 | ||||
| chr17:3668546-3668824 | Common:2; Rare:109 | ||||
| chr17:3723802-3723932 | Rare:75 | ||||
| chr17:4143010-4143225 | Rare:71 | ||||
| chr17:4263948-4264072 | Rare:51 | ||||
| chr17:4555312-4555525 | Common:3; Rare:99 | ||||
| chr17:4704117-4704189 | Rare:40 | ||||
| chr17:4738531-4738855 | Common:3; Rare:75 | ||||
| chr17:4807014-4807203 | Common:4; Rare:60 | ||||
| chr17:4833211-4833416 | Rare:66 | ||||
| chr17:4939916-4940129 | Common:2; Rare:71 | ||||
| chr17:4948948-4949177 | Common:2; Rare:82 | ||||
| chr17:4967781-4967909 | Rare:50 | ||||
| chr17:5191838-5192073 | Common:1; Rare:79 | ||||
| chr17:5419651-5419863 | Common:3; Rare:62 |