| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7931906-7932242 | Common:5; Rare:92 | ||||
| chr17:8151172-8151500 | Common:3; Rare:82 | ||||
| chr17:8152340-8152719 | Common:4; Rare:91 | ||||
| chr17:8162881-8163082 | Common:1; Rare:65 | ||||
| chr17:8248037-8248119 | Common:2; Rare:42; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249226-8249325 | Common:1; Rare:31 | ||||
| chr17:8965673-8965789 | Common:1; Rare:34 | ||||
| chr17:10036576-10037074 | Common:5; Rare:89 | ||||
| chr17:10697374-10697653 | Common:3; Rare:122; Clinvar:5; Clinvar (benign):6 | ||||
| chr17:14069384-14069608 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:15260684-15260961 | Common:1; Rare:98; Clinvar (benign):4 | ||||
| chr17:15262460-15262684 | Rare:50 | ||||
| chr17:15999600-16000028 | Common:3; Rare:182; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16040440-16040666 | Common:2; Rare:37 | ||||
| chr17:17496388-17496575 | Common:2; Rare:51 |