Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1747207-1747356 | Rare:44 | ||||
chr17:1774762-1775198 | Common:3; Rare:150; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr17:1777115-1777280 | Rare:66; Clinvar:1 | ||||
chr17:3664725-3664913 | Rare:40 | ||||
chr17:3664933-3665180 | Common:2; Rare:31 | ||||
chr17:4981352-4981448 | Rare:23 | ||||
chr17:5362710-5362962 | Rare:55 | ||||
chr17:7556871-7557195 | Rare:88; Clinvar (benign):1 | ||||
chr17:7578207-7578485 | Rare:80 | ||||
chr17:7834116-7834256 | Rare:49 | ||||
chr17:7836331-7836451 | Common:1; Rare:39 | ||||
chr17:7887415-7887788 | Common:1; Rare:72 | ||||
chr17:7915892-7916039 | Common:2; Rare:65 | ||||
chr17:8154518-8154639 | Rare:21 | ||||
chr17:8222558-8222676 | Common:2; Rare:27 |