Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:64914224-64914513 | Common:3; Rare:107 | ||||
chr14:65411659-65411921 | Common:3; Rare:65 | ||||
chr14:65412547-65412918 | Common:6; Rare:120 | ||||
chr14:66507819-66508112 | Rare:116 | ||||
chr14:67359770-67360030 | Rare:87 | ||||
chr14:67816572-67816727 | Rare:29 | ||||
chr14:69398248-69398430 | Common:1; Rare:72 | ||||
chr14:69398595-69398723 | Rare:31 | ||||
chr14:69611478-69611708 | Common:1; Rare:80 | ||||
chr14:70416971-70417124 | Rare:49 | ||||
chr14:71320308-71320507 | Rare:62 | ||||
chr14:73058296-73058588 | Common:3; Rare:89 | ||||
chr14:73644849-73645016 | Common:3; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
chr14:73886785-73886893 | Common:2; Rare:36 | ||||
chr14:73950086-73950323 | Common:5; Rare:93; Clinvar (benign):3 |