| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63821576-63821846 | Rare:102 | ||||
| chr17:63827057-63827528 | Common:5; Rare:139 | ||||
| chr17:63837197-63837562 | Rare:93 | ||||
| chr17:64505368-64505544 | Common:2; Rare:66 | ||||
| chr17:64506075-64506428 | Common:4; Rare:171 | ||||
| chr17:64506512-64506812 | Common:3; Rare:114 | ||||
| chr17:64919459-64919570 | Common:5; Rare:14 | ||||
| chr17:65056520-65057011 | Common:5; Rare:202 | ||||
| chr17:67245150-67245383 | Rare:74 | ||||
| chr17:67717740-67717956 | Rare:70 | ||||
| chr17:67826246-67826471 | Common:2; Rare:59 | ||||
| chr17:68247882-68248147 | Common:6; Rare:107 | ||||
| chr17:68512386-68512524 | Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:68601368-68601635 | Common:5; Rare:72 | ||||
| chr17:69141787-69142147 | Common:2; Rare:74 |