| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43125260-43125713 | Rare:120; Clinvar:7; Clinvar (benign):8 | ||||
| chr17:43170088-43170548 | Common:3; Rare:100 | ||||
| chr17:43170925-43171268 | Common:1; Rare:117 | ||||
| chr17:43211605-43212092 | Common:4; Rare:106 | ||||
| chr17:43212304-43212342 | Rare:9 | ||||
| chr17:43398868-43399024 | Common:1; Rare:50 | ||||
| chr17:43483583-43484129 | Rare:147 | ||||
| chr17:43484214-43484329 | Common:3; Rare:30 | ||||
| chr17:43545549-43545854 | Common:2; Rare:83 | ||||
| chr17:43546280-43546670 | Common:2; Rare:90 | ||||
| chr17:43778843-43778982 | Rare:38 | ||||
| chr17:43900602-43900758 | Rare:48 | ||||
| chr17:44014881-44015108 | Common:2; Rare:72 | ||||
| chr17:44066252-44066407 | Rare:48 | ||||
| chr17:44066597-44066798 | Common:1; Rare:82 |