| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64129964-64129985 | Rare:3 | ||||
| chr17:64130027-64130455 | Common:7; Rare:108 | ||||
| chr17:64130649-64130775 | Rare:24 | ||||
| chr17:64263216-64263503 | Common:2; Rare:102 | ||||
| chr17:64263674-64263732 | Rare:12 | ||||
| chr17:64496741-64496830 | Rare:36; Clinvar (benign):1 | ||||
| chr17:64496974-64497242 | Common:3; Rare:137; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:64505497-64505655 | Rare:46 | ||||
| chr17:64505839-64505897 | Common:3; Rare:22 | ||||
| chr17:64506043-64506462 | Common:5; Rare:195 | ||||
| chr17:64506581-64506913 | Common:4; Rare:128 | ||||
| chr17:64506915-64507142 | Common:1; Rare:104 | ||||
| chr17:64507278-64507348 | Rare:22 | ||||
| chr17:64507437-64507788 | Common:1; Rare:98 | ||||
| chr17:64661987-64662143 | Rare:60 |