| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44899375-44899741 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:45060987-45061332 | Common:2; Rare:91 | ||||
| chr17:45148150-45148478 | Common:1; Rare:94 | ||||
| chr17:46192859-46193019 | Common:1; Rare:43 | ||||
| chr17:47188843-47188903 | Rare:7 | ||||
| chr17:47189250-47189568 | Rare:81 | ||||
| chr17:47323894-47323987 | Common:1; Rare:25 | ||||
| chr17:47831508-47831746 | Rare:67 | ||||
| chr17:47941368-47941621 | Rare:52; Clinvar:1 | ||||
| chr17:48048039-48048397 | Common:1; Rare:97 | ||||
| chr17:48590207-48590428 | Common:1; Rare:48 | ||||
| chr17:48944783-48944850 | Rare:18 | ||||
| chr17:49210228-49210413 | Common:2; Rare:27 | ||||
| chr17:49210427-49210712 | Common:1; Rare:53 | ||||
| chr17:49788577-49788745 | Common:1; Rare:52 |