Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:68796194-68796265 | Rare:23 | ||||
chr14:69398586-69398695 | Rare:26 | ||||
chr14:70416977-70417116 | Rare:45 | ||||
chr14:70907293-70907580 | Common:2; Rare:114 | ||||
chr14:71320365-71320495 | Rare:45 | ||||
chr14:71320914-71321165 | Common:2; Rare:88 | ||||
chr14:73058303-73058595 | Common:3; Rare:91 | ||||
chr14:73136309-73136541 | Common:4; Rare:74; Clinvar:4; Clinvar (benign):1 | ||||
chr14:73760265-73760512 | Common:2; Rare:48 | ||||
chr14:73787124-73787379 | Common:2; Rare:88 | ||||
chr14:73851899-73851921 | Rare:7 | ||||
chr14:73950130-73950322 | Common:4; Rare:79; Clinvar (benign):2 | ||||
chr14:74019263-74019389 | Common:1; Rare:51 | ||||
chr14:74493570-74493770 | Common:3; Rare:76; Clinvar (benign):4 | ||||
chr14:74713078-74713228 | Rare:74 |