| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1649310-1649690 | Common:5; Rare:237 | ||||
| chr17:1649786-1650279 | Common:12; Rare:583 | ||||
| chr17:1650829-1651139 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:1683679-1684660 | Common:21; Rare:564; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:1684743-1685164 | Common:18; Rare:725; Clinvar:47; Clinvar (benign):7 | ||||
| chr17:1710160-1710590 | Rare:328 | ||||
| chr17:1710590-1710830 | Rare:90 | ||||
| chr17:1716181-1716781 | Common:16; Rare:546 | ||||
| chr17:1716694-1717352 | Common:3; Rare:224 | ||||
| chr17:1724450-1724955 | Common:10; Rare:454 | ||||
| chr17:1725019-1725874 | Rare:482 | ||||
| chr17:1730140-1730670 | Common:4; Rare:303 | ||||
| chr17:1730913-1731360 | Common:2; Rare:335; Clinvar (pathogenic):4 | ||||
| chr17:1761805-1762205 | Common:4; Rare:171; Clinvar:3; Clinvar (benign):4 | ||||
| chr17:1762471-1762835 | Common:12; Rare:215 |