| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59154974-59155862 | Common:9; Rare:1050 | ||||
| chr17:59209601-59210179 | Common:12; Rare:678 | ||||
| chr17:59210116-59210516 | Rare:130 | ||||
| chr17:59220309-59220893 | Common:20; Rare:587 | ||||
| chr17:59331320-59331753 | Common:5; Rare:252 | ||||
| chr17:59565310-59565710 | Common:3; Rare:315 | ||||
| chr17:59565853-59566253 | Rare:152 | ||||
| chr17:59618852-59619509 | Common:20; Rare:426 | ||||
| chr17:59619440-59620150 | Common:22; Rare:1155 | ||||
| chr17:59706067-59707099 | Common:10; Rare:323 | ||||
| chr17:59707130-59707300 | Common:2; Rare:33 | ||||
| chr17:59707319-59707765 | Common:25; Rare:712; Clinvar (benign):35 | ||||
| chr17:59837570-59838100 | Common:2; Rare:432 | ||||
| chr17:59838334-59838837 | Common:1; Rare:164 | ||||
| chr17:59892644-59893239 | Common:4; Rare:752 |