| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68292019-68292193 | Common:3; Rare:53 | ||||
| chr17:68378179-68378422 | Common:1; Rare:62 | ||||
| chr17:68413572-68413763 | Common:1; Rare:53 | ||||
| chr17:68424925-68425057 | Common:1; Rare:20 | ||||
| chr17:68498940-68499096 | Rare:20 | ||||
| chr17:68554816-68554923 | Common:1; Rare:21; Clinvar (pathogenic):1 | ||||
| chr17:75039415-75039514 | Rare:13 | ||||
| chr17:75136207-75136464 | Common:3; Rare:63 | ||||
| chr17:75295665-75296002 | Common:5; Rare:44 | ||||
| chr17:75501632-75501808 | Common:1; Rare:65 | ||||
| chr17:75603877-75603955 | Common:1; Rare:13 | ||||
| chr17:75722178-75722342 | Rare:26 | ||||
| chr17:75723402-75723411 | Rare:1 | ||||
| chr17:75756304-75756488 | Rare:60; Clinvar (benign):1 | ||||
| chr17:75822354-75822657 | Rare:64 |