| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1485720-1486071 | Common:4; Rare:117 | ||||
| chr17:1486904-1487014 | Rare:25 | ||||
| chr17:1491608-1491816 | Common:1; Rare:63 | ||||
| chr17:1492655-1492707 | Rare:9 | ||||
| chr17:1513519-1513651 | Rare:42 | ||||
| chr17:1516582-1516984 | Common:2; Rare:143 | ||||
| chr17:1628374-1628391 | Rare:4 | ||||
| chr17:1628782-1629011 | Rare:81 | ||||
| chr17:1645702-1645828 | Common:1; Rare:38 | ||||
| chr17:1648906-1649212 | Common:2; Rare:97 | ||||
| chr17:1661660-1661972 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:1684780-1685036 | Common:2; Rare:87; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1710342-1710463 | Rare:31 | ||||
| chr17:1716114-1716538 | Common:3; Rare:131 | ||||
| chr17:1724673-1724969 | Common:2; Rare:91 |