| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64263166-64263482 | Common:2; Rare:103 | ||||
| chr17:64390661-64390869 | Common:1; Rare:29 | ||||
| chr17:64496989-64497147 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:64505365-64505800 | Common:7; Rare:163 | ||||
| chr17:64505827-64506470 | Common:15; Rare:290 | ||||
| chr17:64506488-64506785 | Common:3; Rare:108 | ||||
| chr17:64662314-64662477 | Common:1; Rare:84 | ||||
| chr17:64919430-64919676 | Common:6; Rare:56 | ||||
| chr17:65056490-65056965 | Common:5; Rare:189 | ||||
| chr17:65137223-65137462 | Common:2; Rare:75 | ||||
| chr17:65826394-65826588 | Rare:33 | ||||
| chr17:65941479-65941606 | Common:1; Rare:21 | ||||
| chr17:66191808-66191918 | Rare:27 | ||||
| chr17:66192037-66192302 | Common:1; Rare:81 | ||||
| chr17:67239432-67239757 | Rare:50 |