| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76726394-76726989 | Common:15; Rare:594 | ||||
| chr17:76737096-76738168 | Common:27; Rare:915 | ||||
| chr17:77088559-77088864 | Common:5; Rare:217 | ||||
| chr17:77140434-77141057 | Common:13; Rare:533 | ||||
| chr17:77280066-77280927 | Common:7; Rare:257 | ||||
| chr17:77281108-77281722 | Common:18; Rare:535 | ||||
| chr17:77285190-77286458 | Common:14; Rare:423 | ||||
| chr17:77286540-77287100 | Common:4; Rare:108 | ||||
| chr17:77287602-77288019 | Rare:138 | ||||
| chr17:77401610-77402635 | Common:5; Rare:529; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr17:78040926-78041099 | Common:4; Rare:84 | ||||
| chr17:78126262-78126890 | Rare:321; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr17:78127130-78128208 | Common:5; Rare:288 | ||||
| chr17:78128208-78128382 | Common:2; Rare:93 | ||||
| chr17:78128569-78128927 | Common:14; Rare:141 |