| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3668571-3668824 | Common:1; Rare:98 | ||||
| chr17:3723776-3723925 | Common:1; Rare:81 | ||||
| chr17:4263948-4264096 | Rare:60 | ||||
| chr17:4939916-4940136 | Common:2; Rare:74 | ||||
| chr17:5419651-5419864 | Common:3; Rare:63 | ||||
| chr17:5486165-5486399 | Common:4; Rare:99 | ||||
| chr17:6640683-6641064 | Common:7; Rare:111 | ||||
| chr17:6651586-6651734 | Common:1; Rare:42 | ||||
| chr17:7012323-7012671 | Rare:120 | ||||
| chr17:7251967-7252311 | Common:1; Rare:132 | ||||
| chr17:7404093-7404310 | Common:1; Rare:56 | ||||
| chr17:7583551-7583858 | Common:1; Rare:126; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7931869-7932239 | Common:5; Rare:97 | ||||
| chr17:10697510-10697637 | Common:3; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:14069481-14069536 | Common:1; Rare:17; Clinvar (benign):2 |