| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77287813-77287993 | Rare:25 | ||||
| chr17:77319434-77319573 | Common:3; Rare:34; Clinvar (benign):3 | ||||
| chr17:77319860-77319927 | Rare:17 | ||||
| chr17:77375867-77375952 | Rare:14 | ||||
| chr17:77375954-77376287 | Common:4; Rare:63 | ||||
| chr17:77450529-77450785 | Rare:50 | ||||
| chr17:77450796-77450830 | Rare:3 | ||||
| chr17:77451260-77451467 | Rare:46 | ||||
| chr17:77497125-77497292 | Rare:33 | ||||
| chr17:78186540-78186763 | Common:8; Rare:51 | ||||
| chr17:78186791-78187411 | Common:4; Rare:203 | ||||
| chr17:78378379-78378649 | Common:1; Rare:66 | ||||
| chr17:78379120-78379326 | Rare:45 | ||||
| chr17:78840300-78840352 | Common:1; Rare:14 | ||||
| chr17:78840498-78841180 | Common:2; Rare:239 |