Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:128394990-128395277 | Common:3; Rare:81; Clinvar:4; Clinvar (benign):2 | ||||
chr7:128409942-128410044 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
chr7:128455663-128455931 | Common:3; Rare:135 | ||||
chr7:128739091-128739419 | Common:3; Rare:98 | ||||
chr7:129054861-129055234 | Common:2; Rare:72 | ||||
chr7:129611616-129611784 | Common:1; Rare:55 | ||||
chr7:130205377-130205507 | Rare:60 | ||||
chr7:131109834-131110101 | Common:1; Rare:49 | ||||
chr7:131285213-131285314 | Common:1; Rare:14 | ||||
chr7:131327309-131327433 | Rare:26 | ||||
chr7:131327688-131327909 | Rare:67 | ||||
chr7:134646566-134646873 | Common:6; Rare:92 | ||||
chr7:134940815-134941280 | Common:4; Rare:96 | ||||
chr7:134986292-134986559 | Common:5; Rare:88 | ||||
chr7:135148013-135148122 | Rare:29 |