Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:218399504-218399760 | Common:1; Rare:116 | ||||
chr2:218568286-218568659 | Common:3; Rare:99 | ||||
chr2:218568733-218568933 | Common:1; Rare:53 | ||||
chr2:218659312-218659738 | Common:4; Rare:99 | ||||
chr2:218671972-218672086 | Rare:39 | ||||
chr2:219176824-219177119 | Common:4; Rare:88 | ||||
chr2:219178142-219178447 | Common:6; Rare:132 | ||||
chr2:219206683-219206923 | Rare:87 | ||||
chr2:219229549-219229900 | Common:2; Rare:112 | ||||
chr2:219245424-219245531 | Rare:33 | ||||
chr2:219253869-219254082 | Common:2; Rare:64 | ||||
chr2:219279240-219279535 | Common:2; Rare:100 | ||||
chr2:219418413-219419080 | Common:6; Rare:221; Clinvar:40; Clinvar (benign):24; Clinvar (pathogenic):3 | ||||
chr2:219419845-219420165 | Common:2; Rare:66; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr2:219441934-219442073 | Rare:29 |