| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45490708-45490921 | Common:6; Rare:70 | ||||
| chr17:46193309-46193597 | Common:5; Rare:78 | ||||
| chr17:46225353-46225463 | Common:1; Rare:31 | ||||
| chr17:46923084-46923174 | Common:1; Rare:35; Clinvar (benign):6 | ||||
| chr17:47189181-47189627 | Common:1; Rare:122 | ||||
| chr17:47323864-47324025 | Common:1; Rare:60 | ||||
| chr17:47649248-47649439 | Rare:54 | ||||
| chr17:47649614-47649931 | Common:1; Rare:118 | ||||
| chr17:47650135-47650238 | Rare:35 | ||||
| chr17:47831516-47831614 | Rare:28 | ||||
| chr17:47841244-47841382 | Rare:26 | ||||
| chr17:47941335-47941607 | Rare:54; Clinvar:1 | ||||
| chr17:47970825-47971157 | Common:1; Rare:76 | ||||
| chr17:48048058-48048397 | Rare:90 | ||||
| chr17:48055852-48055977 | Rare:25 |