| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:410659-410778 | Common:2; Rare:37 | ||||
| chr17:714024-714315 | Common:2; Rare:60 | ||||
| chr17:714740-714982 | Common:4; Rare:73; Clinvar (benign):1 | ||||
| chr17:715321-715658 | Common:3; Rare:58 | ||||
| chr17:732077-732242 | Rare:54 | ||||
| chr17:732292-732709 | Common:2; Rare:144 | ||||
| chr17:732995-733207 | Common:4; Rare:86 | ||||
| chr17:751551-751668 | Rare:27 | ||||
| chr17:751745-751850 | Rare:30 | ||||
| chr17:751881-752037 | Common:1; Rare:43 | ||||
| chr17:752132-752523 | Common:3; Rare:152 | ||||
| chr17:752583-752902 | Common:2; Rare:80 | ||||
| chr17:781960-782033 | Common:1; Rare:23 | ||||
| chr17:782179-782468 | Common:2; Rare:155 | ||||
| chr17:979752-980002 | Common:1; Rare:109 |