Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:67359738-67360023 | Common:1; Rare:91 | ||||
chr14:67360062-67360391 | Common:4; Rare:83 | ||||
chr14:67412114-67412365 | Common:1; Rare:55 | ||||
chr14:67674564-67674932 | Common:1; Rare:91 | ||||
chr14:67816578-67816732 | Rare:27 | ||||
chr14:68793049-68793363 | Common:1; Rare:66 | ||||
chr14:69398253-69398421 | Rare:67 | ||||
chr14:69398595-69398747 | Rare:36 | ||||
chr14:71320319-71320487 | Rare:50 | ||||
chr14:73058249-73058579 | Common:3; Rare:104 | ||||
chr14:73569061-73569286 | Rare:54 | ||||
chr14:73787175-73787379 | Common:2; Rare:75 | ||||
chr14:73851752-73851860 | Common:1; Rare:30 | ||||
chr14:73886785-73886893 | Common:2; Rare:36 | ||||
chr14:73950092-73950330 | Common:5; Rare:97; Clinvar (benign):3 |