| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:10729749-10729816 | Rare:36 | ||||
| chr17:10729972-10730107 | Common:3; Rare:33 | ||||
| chr17:11997450-11997594 | Rare:49 | ||||
| chr17:14069360-14069580 | Common:2; Rare:81; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:14300830-14301105 | Common:2; Rare:77 | ||||
| chr17:15260756-15260928 | Rare:65; Clinvar (benign):2 | ||||
| chr17:15262460-15262634 | Rare:38 | ||||
| chr17:15563449-15563782 | Common:1; Rare:110 | ||||
| chr17:15699541-15699773 | Common:3; Rare:65 | ||||
| chr17:15999628-16000158 | Common:4; Rare:214; Clinvar:6; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr17:16217102-16217227 | Rare:31 | ||||
| chr17:16380572-16380829 | Common:4; Rare:67 | ||||
| chr17:16653813-16654035 | Rare:57 | ||||
| chr17:17591589-17591926 | Common:2; Rare:96 | ||||
| chr17:18087829-18088026 | Rare:52 |