Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27628981-27629054 | Common:1; Rare:36 | ||||
chr2:27663369-27663469 | Rare:28 | ||||
chr2:27663578-27663911 | Rare:119 | ||||
chr2:27890425-27890764 | Rare:83 | ||||
chr2:28751728-28752134 | Common:1; Rare:166 | ||||
chr2:28870267-28870448 | Rare:69 | ||||
chr2:30146600-30147019 | Common:5; Rare:134 | ||||
chr2:32039747-32039851 | Rare:34 | ||||
chr2:32165665-32165886 | Common:1; Rare:80 | ||||
chr2:32627956-32628123 | Rare:53 | ||||
chr2:33134220-33134526 | Common:3; Rare:73 | ||||
chr2:37084276-37084559 | Common:3; Rare:105 | ||||
chr2:37231519-37231696 | Common:5; Rare:98; Clinvar (benign):3 | ||||
chr2:38076149-38076282 | Rare:35 | ||||
chr2:38751307-38751595 | Common:5; Rare:141 |