| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:6651574-6651668 | Common:1; Rare:25 | ||||
| chr17:7012323-7012678 | Rare:123 | ||||
| chr17:7223307-7223544 | Rare:64 | ||||
| chr17:7234472-7234679 | Common:2; Rare:108 | ||||
| chr17:7251967-7252311 | Common:1; Rare:132 | ||||
| chr17:7352054-7352162 | Rare:36 | ||||
| chr17:7479557-7479713 | Rare:25 | ||||
| chr17:7484239-7484370 | Common:1; Rare:53 | ||||
| chr17:7484617-7484834 | Common:1; Rare:94 | ||||
| chr17:7583550-7583858 | Common:1; Rare:126; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7584077-7584191 | Rare:24 | ||||
| chr17:7627792-7627971 | Common:2; Rare:58 | ||||
| chr17:7857170-7857365 | Common:1; Rare:105 | ||||
| chr17:7857467-7857776 | Common:2; Rare:98 | ||||
| chr17:7888713-7888829 | Rare:30 |