Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:105854403-105855242 | Common:3; Rare:254 | ||||
chr14:105855478-105855836 | Common:3; Rare:127 | ||||
chr14:105855899-105856074 | Common:2; Rare:59; Clinvar (benign):1 | ||||
chr14:105856076-105856188 | Common:1; Rare:35; Clinvar (benign):1 | ||||
chr14:105856205-105856376 | Common:3; Rare:58 | ||||
chr14:105856668-105856695 | Rare:2 | ||||
chr14:105856969-105857072 | Rare:15 | ||||
chr14:105857120-105857412 | Common:2; Rare:68 | ||||
chr14:105857574-105857722 | Common:2; Rare:47 | ||||
chr14:105861002-105861094 | Rare:48 | ||||
chr14:105861900-105862373 | Common:4; Rare:194 | ||||
chr14:105862663-105862782 | Common:3; Rare:78 | ||||
chr14:105863261-105863325 | Rare:90 | ||||
chr14:106185228-106185487 | Common:1; Rare:134 | ||||
chr14:106185984-106186146 | Common:2; Rare:27 |