Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1829791-1830039 | Common:7; Rare:107 | ||||
chr17:2303770-2303973 | Common:2; Rare:71 | ||||
chr17:2511844-2511995 | Common:2; Rare:42 | ||||
chr17:3636246-3636501 | Common:4; Rare:70; Clinvar (benign):1 | ||||
chr17:3668552-3668824 | Common:2; Rare:106 | ||||
chr17:3723802-3723925 | Rare:68 | ||||
chr17:4263947-4264072 | Rare:51 | ||||
chr17:4555338-4555525 | Common:3; Rare:85 | ||||
chr17:4704117-4704201 | Rare:53 | ||||
chr17:4807011-4807192 | Common:4; Rare:61 | ||||
chr17:4939912-4940140 | Common:2; Rare:76 | ||||
chr17:4948945-4949129 | Common:1; Rare:62 | ||||
chr17:4951031-4951119 | Common:1; Rare:23; Clinvar (benign):1 | ||||
chr17:4967797-4967900 | Rare:42 | ||||
chr17:5419636-5419869 | Common:3; Rare:72 |