Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:92040016-92040140 | Common:2; Rare:42; Clinvar:3; Clinvar (benign):1 | ||||
chr14:92121658-92122017 | Common:4; Rare:124 | ||||
chr14:92122064-92122229 | Rare:38 | ||||
chr14:92513724-92513846 | Common:1; Rare:27 | ||||
chr14:93184845-93185027 | Rare:64 | ||||
chr14:93207053-93207327 | Common:3; Rare:140 | ||||
chr14:93333003-93333180 | Common:1; Rare:66 | ||||
chr14:93976547-93976881 | Rare:63 | ||||
chr14:94081130-94081402 | Common:5; Rare:82 | ||||
chr14:94129556-94129689 | Common:3; Rare:49 | ||||
chr14:95157343-95157688 | Common:4; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
chr14:95534573-95534653 | Rare:34 | ||||
chr14:95534749-95535092 | Common:4; Rare:114; Clinvar (benign):4 | ||||
chr14:96255501-96255926 | Common:1; Rare:66 | ||||
chr14:96363308-96363559 | Common:1; Rare:86 |