| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50192795-50193048 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50194539-50194829 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50195018-50195362 | Common:1; Rare:104; Clinvar:1; Clinvar (benign):5 | ||||
| chr17:50195433-50195678 | Rare:53; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50196153-50196539 | Common:2; Rare:113; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:50197948-50198206 | Common:3; Rare:66; Clinvar (benign):6 | ||||
| chr17:50199554-50199954 | Common:7; Rare:133; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50201409-50201804 | Common:2; Rare:116; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:50373160-50373253 | Common:3; Rare:41 | ||||
| chr17:50707632-50707836 | Common:4; Rare:63 | ||||
| chr17:50719463-50719661 | Rare:77 | ||||
| chr17:50866355-50866613 | Common:3; Rare:77 | ||||
| chr17:51153292-51153623 | Common:1; Rare:86 | ||||
| chr17:51260367-51260576 | Common:3; Rare:94 | ||||
| chr17:54968608-54968792 | Common:3; Rare:89 |