| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59619563-59619997 | Common:3; Rare:157 | ||||
| chr17:59620002-59620170 | Rare:47 | ||||
| chr17:59685321-59685655 | Common:2; Rare:69 | ||||
| chr17:59707403-59707747 | Common:3; Rare:93; Clinvar (benign):2 | ||||
| chr17:59838423-59838739 | Rare:56 | ||||
| chr17:59892884-59893239 | Common:1; Rare:111 | ||||
| chr17:59964706-59965096 | Common:2; Rare:119 | ||||
| chr17:60078903-60078941 | Common:3; Rare:24 | ||||
| chr17:60392123-60392438 | Common:3; Rare:81 | ||||
| chr17:60526082-60526290 | Rare:76 | ||||
| chr17:60600023-60600224 | Common:3; Rare:66 | ||||
| chr17:62065249-62065431 | Common:4; Rare:61 | ||||
| chr17:63446262-63446531 | Rare:87 | ||||
| chr17:63477102-63477493 | Common:2; Rare:166; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:63483457-63483969 | Common:5; Rare:159; Clinvar:4; Clinvar (pathogenic):2 |