| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63827051-63827738 | Common:7; Rare:198 | ||||
| chr17:64662297-64662493 | Common:1; Rare:94 | ||||
| chr17:65056579-65056930 | Common:4; Rare:141 | ||||
| chr17:67245165-67245492 | Rare:105 | ||||
| chr17:68247817-68248137 | Common:6; Rare:143 | ||||
| chr17:72120760-72121029 | Rare:68 | ||||
| chr17:73232137-73232403 | Common:1; Rare:129 | ||||
| chr17:73311982-73312215 | Rare:62 | ||||
| chr17:74748417-74748635 | Common:2; Rare:73 | ||||
| chr17:74776329-74776540 | Common:4; Rare:66 | ||||
| chr17:75012362-75012696 | Common:1; Rare:68 | ||||
| chr17:75046929-75047154 | Common:1; Rare:68 | ||||
| chr17:75205379-75205730 | Common:1; Rare:104 | ||||
| chr17:75261590-75261925 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr17:75271159-75271375 | Common:2; Rare:39 |