Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8176313-8176441 | Rare:44 | ||||
chr17:8248037-8248101 | Rare:38; Clinvar:2 | ||||
chr17:8965667-8965806 | Common:1; Rare:39 | ||||
chr17:10036480-10037074 | Common:5; Rare:105 | ||||
chr17:10697485-10697654 | Common:3; Rare:75; Clinvar:5; Clinvar (benign):2 | ||||
chr17:10729590-10729801 | Common:3; Rare:79 | ||||
chr17:10729980-10730128 | Common:3; Rare:31 | ||||
chr17:14069395-14069565 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15260621-15260922 | Rare:108; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr17:15262415-15262748 | Rare:76 | ||||
chr17:15265153-15265447 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15699559-15699773 | Common:3; Rare:60 | ||||
chr17:15999590-15999824 | Common:1; Rare:122; Clinvar:4; Clinvar (benign):4 | ||||
chr17:16039730-16039932 | Common:1; Rare:40 | ||||
chr17:16215530-16215606 | Rare:29 |