| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76726410-76726910 | Common:10; Rare:359 | ||||
| chr17:76737124-76737732 | Common:12; Rare:467 | ||||
| chr17:76737831-76738121 | Common:8; Rare:157 | ||||
| chr17:76872320-76872990 | Common:4; Rare:297 | ||||
| chr17:77088606-77088869 | Common:4; Rare:144 | ||||
| chr17:77140606-77141057 | Common:7; Rare:313 | ||||
| chr17:77281151-77281530 | Common:9; Rare:305 | ||||
| chr17:77287748-77288037 | Rare:71 | ||||
| chr17:77319434-77319717 | Common:6; Rare:132; Clinvar:2; Clinvar (benign):6 | ||||
| chr17:77320020-77320293 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:78040838-78041096 | Common:2; Rare:63 | ||||
| chr17:78127150-78127560 | Common:6; Rare:134 | ||||
| chr17:78128222-78128329 | Rare:20 | ||||
| chr17:78128591-78128914 | Common:14; Rare:148 | ||||
| chr17:78168526-78168630 | Rare:67 |