| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1562653-1563026 | Common:3; Rare:109 | ||||
| chr17:1628343-1628599 | Rare:86 | ||||
| chr17:1628739-1629101 | Common:1; Rare:116 | ||||
| chr17:1649148-1649299 | Common:1; Rare:64 | ||||
| chr17:1649464-1649528 | Common:1; Rare:24 | ||||
| chr17:1650061-1650172 | Rare:34 | ||||
| chr17:1684395-1684521 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:1684665-1685082 | Common:2; Rare:139; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1710282-1710802 | Rare:130 | ||||
| chr17:1716158-1716828 | Common:5; Rare:206 | ||||
| chr17:1716832-1717405 | Common:2; Rare:118 | ||||
| chr17:1724542-1724802 | Common:2; Rare:91 | ||||
| chr17:1725093-1725123 | Rare:10 | ||||
| chr17:1742682-1742891 | Rare:43 | ||||
| chr17:1769979-1770491 | Common:4; Rare:132; Clinvar:1; Clinvar (benign):2 |