| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75784563-75784875 | Common:2; Rare:139 | ||||
| chr17:75855293-75855647 | Common:1; Rare:94 | ||||
| chr17:75904860-75905017 | Common:2; Rare:54 | ||||
| chr17:75979055-75979298 | Rare:69; Clinvar:4 | ||||
| chr17:75979386-75979581 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr17:76072495-76072664 | Rare:50 | ||||
| chr17:76103695-76103876 | Common:5; Rare:64 | ||||
| chr17:76353605-76353668 | Rare:25 | ||||
| chr17:76353838-76353942 | Rare:45 | ||||
| chr17:76501406-76501572 | Rare:49; Clinvar (benign):2 | ||||
| chr17:76725764-76726091 | Common:1; Rare:92 | ||||
| chr17:76726458-76726914 | Common:5; Rare:178 | ||||
| chr17:76737314-76737687 | Common:4; Rare:131 | ||||
| chr17:76737870-76738129 | Common:4; Rare:75 | ||||
| chr17:77088547-77088762 | Common:1; Rare:56 |