| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63405975-63406284 | Common:1; Rare:74 | ||||
| chr17:63414423-63414607 | Rare:26 | ||||
| chr17:63415359-63415602 | Rare:54 | ||||
| chr17:63483504-63483658 | Common:5; Rare:45; Clinvar:1 | ||||
| chr17:63490937-63491262 | Common:2; Rare:125; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:63506763-63506880 | Common:1; Rare:21 | ||||
| chr17:64145765-64145990 | Common:2; Rare:61 | ||||
| chr17:64179113-64179428 | Common:6; Rare:57 | ||||
| chr17:64781978-64782121 | Rare:24 | ||||
| chr17:64837097-64837348 | Common:1; Rare:70 | ||||
| chr17:64975011-64975328 | Common:2; Rare:66 | ||||
| chr17:64975434-64975741 | Common:3; Rare:108 | ||||
| chr17:64977539-64977682 | Common:2; Rare:22 | ||||
| chr17:65100693-65100906 | Rare:66 | ||||
| chr17:65537841-65538186 | Common:11; Rare:179; Clinvar (benign):5 |