| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75979091-75979328 | Rare:67; Clinvar:4 | ||||
| chr17:76103712-76103867 | Common:4; Rare:49 | ||||
| chr17:76353605-76353865 | Common:2; Rare:94 | ||||
| chr17:76501385-76501522 | Rare:49; Clinvar (benign):3 | ||||
| chr17:76726433-76726874 | Common:5; Rare:160 | ||||
| chr17:77319402-77319602 | Common:3; Rare:52; Clinvar (benign):3 | ||||
| chr17:77320077-77320323 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78040837-78040917 | Rare:13 | ||||
| chr17:78168516-78168611 | Rare:26 | ||||
| chr17:78187029-78187365 | Common:3; Rare:109 | ||||
| chr17:78840783-78841004 | Common:1; Rare:83 | ||||
| chr17:78979872-78980201 | Common:2; Rare:66 | ||||
| chr17:79009696-79009938 | Common:9; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:80035849-80035989 | Common:1; Rare:50 | ||||
| chr17:80220314-80220453 | Rare:54; Clinvar:1 |