Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:93232201-93232420 | Common:3; Rare:45 | ||||
chr7:94425746-94426050 | Rare:93; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr7:94656026-94656445 | Common:2; Rare:98; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr7:95596516-95596713 | Common:2; Rare:39 | ||||
chr7:96322037-96322119 | Rare:46; Clinvar:4 | ||||
chr7:98252136-98252364 | Common:1; Rare:52 | ||||
chr7:99408534-99408983 | Common:3; Rare:127 | ||||
chr7:99438696-99439002 | Common:1; Rare:101 | ||||
chr7:99472646-99472912 | Common:4; Rare:83 | ||||
chr7:99500238-99500417 | Common:2; Rare:50 | ||||
chr7:99552075-99552170 | Rare:34 | ||||
chr7:99558519-99558860 | Common:3; Rare:98 | ||||
chr7:100101333-100101677 | Common:1; Rare:131 | ||||
chr7:100119335-100119717 | Rare:111 | ||||
chr7:100148718-100149017 | Common:1; Rare:129 |