Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:128405925-128406135 | Common:2; Rare:75 | ||||
chr7:128409908-128410076 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
chr7:128455729-128455921 | Common:2; Rare:108 | ||||
chr7:128830186-128830456 | Common:4; Rare:74 | ||||
chr7:129054884-129055239 | Common:2; Rare:68 | ||||
chr7:129434248-129434467 | Common:1; Rare:80 | ||||
chr7:129611600-129611783 | Common:2; Rare:61 | ||||
chr7:130070302-130070572 | Common:1; Rare:73 | ||||
chr7:130205377-130205525 | Rare:69 | ||||
chr7:131109892-131110064 | Rare:28 | ||||
chr7:131327737-131327899 | Rare:56 | ||||
chr7:134646592-134646856 | Common:5; Rare:75 | ||||
chr7:135147998-135148127 | Rare:33 | ||||
chr7:135170645-135170999 | Common:6; Rare:112 | ||||
chr7:135977270-135977530 | Common:3; Rare:103 |