| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:14300660-14301142 | Common:17; Rare:593 | ||||
| chr17:14301343-14301743 | Common:3; Rare:154 | ||||
| chr17:15260310-15260690 | Common:4; Rare:93; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:15260690-15261115 | Common:11; Rare:481; Clinvar (benign):18 | ||||
| chr17:15261186-15261586 | Common:2; Rare:76 | ||||
| chr17:15262403-15262819 | Rare:298 | ||||
| chr17:15563419-15563875 | Common:5; Rare:660 | ||||
| chr17:15651575-15651989 | Common:2; Rare:214 | ||||
| chr17:15684228-15684343 | Common:3; Rare:39 | ||||
| chr17:15699421-15699823 | Common:26; Rare:547 | ||||
| chr17:15944560-15944860 | Common:4; Rare:163 | ||||
| chr17:15944880-15945320 | Common:9; Rare:305 | ||||
| chr17:15980013-15980413 | Common:4; Rare:95 | ||||
| chr17:15999401-16000202 | Common:25; Rare:1455; Clinvar:42; Clinvar (benign):68; Clinvar (pathogenic):12 | ||||
| chr17:16215370-16215774 | Common:12; Rare:695 |