Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:123601591-123601893 | Rare:65 | ||||
chr7:123748925-123749258 | Common:3; Rare:123 | ||||
chr7:124929800-124929929 | Common:3; Rare:43 | ||||
chr7:128455743-128455903 | Common:2; Rare:90 | ||||
chr7:128830185-128830442 | Common:4; Rare:69 | ||||
chr7:128830581-128830700 | Rare:56; Clinvar:5; Clinvar (benign):2 | ||||
chr7:128830904-128830986 | Rare:21; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr7:129054884-129055209 | Common:1; Rare:64 | ||||
chr7:129434248-129434460 | Common:1; Rare:78 | ||||
chr7:129611616-129611792 | Common:1; Rare:57 | ||||
chr7:131327715-131327905 | Rare:65 | ||||
chr7:134646576-134646916 | Common:7; Rare:109 | ||||
chr7:135170665-135170871 | Common:2; Rare:77 | ||||
chr7:139340397-139340495 | Rare:28 | ||||
chr7:139341234-139341380 | Rare:34 |