| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15260796-15261047 | Common:2; Rare:74; Clinvar (benign):1 | ||||
| chr17:15999590-15999984 | Common:3; Rare:178; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr17:16039557-16039731 | Common:1; Rare:48 | ||||
| chr17:16040440-16040627 | Common:1; Rare:28 | ||||
| chr17:16215532-16215652 | Common:1; Rare:51 | ||||
| chr17:17495650-17495925 | Common:1; Rare:76 | ||||
| chr17:17496388-17496548 | Rare:38 | ||||
| chr17:18039143-18039410 | Common:3; Rare:67; Clinvar (benign):1 | ||||
| chr17:18183069-18183119 | Rare:20 | ||||
| chr17:18183329-18183487 | Rare:33 | ||||
| chr17:18183713-18183925 | Rare:97 | ||||
| chr17:18253405-18253682 | Rare:104 | ||||
| chr17:18254609-18254823 | Rare:70 | ||||
| chr17:18260411-18260668 | Rare:75 | ||||
| chr17:18314921-18315326 | Common:1; Rare:114 |