Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:68878653-68878773 | Rare:40 | ||||
chr14:68977705-68978043 | Common:6; Rare:82 | ||||
chr14:68978107-68978402 | Common:2; Rare:81 | ||||
chr14:68978450-68978463 | Rare:1 | ||||
chr14:68978957-68979587 | Common:3; Rare:176 | ||||
chr14:69398251-69398389 | Rare:61 | ||||
chr14:69398595-69398731 | Rare:33 | ||||
chr14:69611458-69611761 | Common:1; Rare:101 | ||||
chr14:71320143-71320487 | Rare:105 | ||||
chr14:72926202-72926524 | Common:4; Rare:77 | ||||
chr14:73058309-73058659 | Common:3; Rare:105 | ||||
chr14:73463623-73463814 | Common:1; Rare:30 | ||||
chr14:73569046-73569286 | Rare:55 | ||||
chr14:73644881-73645034 | Common:3; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
chr14:73787165-73787349 | Common:2; Rare:72 |