| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79009687-79009947 | Common:9; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:79022607-79022841 | Common:2; Rare:37 | ||||
| chr17:79022915-79023052 | Common:2; Rare:23 | ||||
| chr17:79023824-79024290 | Common:1; Rare:102 | ||||
| chr17:79046645-79046954 | Common:1; Rare:82 | ||||
| chr17:79993783-79993847 | Rare:9 | ||||
| chr17:80035830-80036037 | Common:1; Rare:69 | ||||
| chr17:80036563-80036665 | Common:2; Rare:26; Clinvar (benign):2 | ||||
| chr17:80101365-80101663 | Common:4; Rare:129; Clinvar (benign):4 | ||||
| chr17:80147061-80147360 | Common:5; Rare:122 | ||||
| chr17:80214264-80214564 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:80220289-80220469 | Common:1; Rare:73; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80353825-80354148 | Common:3; Rare:96 | ||||
| chr17:80371687-80371909 | Common:2; Rare:48 | ||||
| chr17:80372819-80373161 | Common:2; Rare:117; Clinvar:1 |