Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:60981037-60981232 | Rare:73 | ||||
chr14:67359773-67360030 | Rare:86 | ||||
chr14:67360062-67360368 | Common:3; Rare:74 | ||||
chr14:69398251-69398426 | Common:1; Rare:69 | ||||
chr14:69398595-69398716 | Rare:30 | ||||
chr14:73058341-73058585 | Common:3; Rare:76 | ||||
chr14:73886777-73886869 | Common:1; Rare:27 | ||||
chr14:74493570-74493770 | Common:3; Rare:76; Clinvar (benign):4 | ||||
chr14:74713083-74713198 | Rare:57 | ||||
chr14:75660789-75661053 | Rare:71 | ||||
chr14:77708000-77708123 | Rare:59 | ||||
chr14:90331913-90332203 | Common:1; Rare:81 | ||||
chr14:92040033-92040168 | Common:2; Rare:31; Clinvar (benign):1 | ||||
chr14:92121673-92121982 | Common:4; Rare:100 | ||||
chr14:93184845-93185001 | Rare:50 |