Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:68793005-68793173 | Rare:52 | ||||
chr14:68794591-68794790 | Common:1; Rare:52 | ||||
chr14:69191413-69191582 | Rare:37 | ||||
chr14:69398230-69398381 | Rare:66 | ||||
chr14:69398595-69398747 | Rare:36 | ||||
chr14:69611458-69611761 | Common:1; Rare:101 | ||||
chr14:69767871-69768195 | Common:2; Rare:92 | ||||
chr14:71320289-71320483 | Rare:60 | ||||
chr14:71320824-71321164 | Common:3; Rare:107 | ||||
chr14:73058303-73058622 | Common:3; Rare:99 | ||||
chr14:73458513-73458847 | Common:4; Rare:86 | ||||
chr14:73568886-73569088 | Common:1; Rare:28 | ||||
chr14:73787166-73787355 | Common:2; Rare:72 | ||||
chr14:73886782-73886902 | Common:2; Rare:40 | ||||
chr14:73950090-73950322 | Common:5; Rare:92; Clinvar (benign):3 |