Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:90595837-90596016 | Common:6; Rare:56 | ||||
chr7:91880672-91880801 | Common:1; Rare:35 | ||||
chr7:92134360-92134890 | Common:5; Rare:154 | ||||
chr7:92245865-92245974 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
chr7:92528439-92528816 | Common:3; Rare:118; Clinvar:3; Clinvar (benign):2 | ||||
chr7:92590047-92590123 | Rare:31 | ||||
chr7:93890599-93890861 | Common:4; Rare:85 | ||||
chr7:93921645-93922135 | Common:7; Rare:109 | ||||
chr7:94004221-94004495 | Rare:78 | ||||
chr7:94394550-94395095 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
chr7:94425743-94426052 | Rare:93; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr7:94656037-94656374 | Common:2; Rare:93; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr7:95596512-95596689 | Common:2; Rare:34 | ||||
chr7:98252197-98252372 | Rare:41 | ||||
chr7:99325784-99325985 | Common:1; Rare:78 |