| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1628802-1629120 | Rare:103 | ||||
| chr17:1644090-1644138 | Rare:8 | ||||
| chr17:1644473-1644765 | Common:3; Rare:53 | ||||
| chr17:1645720-1645918 | Common:2; Rare:43 | ||||
| chr17:1648979-1649264 | Common:3; Rare:99 | ||||
| chr17:1649490-1649662 | Common:2; Rare:65 | ||||
| chr17:1684402-1684495 | Common:1; Rare:41 | ||||
| chr17:1684786-1685115 | Common:4; Rare:105; Clinvar:6; Clinvar (benign):1 | ||||
| chr17:1716113-1716714 | Common:5; Rare:188 | ||||
| chr17:1716992-1717360 | Common:1; Rare:76 | ||||
| chr17:1724526-1724843 | Common:2; Rare:108 | ||||
| chr17:1725301-1725434 | Rare:34 | ||||
| chr17:1783909-1784003 | Rare:15 | ||||
| chr17:1829731-1830106 | Common:9; Rare:153 | ||||
| chr17:2029929-2030217 | Common:3; Rare:111; Clinvar (pathogenic):1 |