Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73851731-73852013 | Common:6; Rare:91 | ||||
chr14:73886735-73886905 | Common:2; Rare:61 | ||||
chr14:73950112-73950333 | Common:5; Rare:88; Clinvar (benign):3 | ||||
chr14:74019264-74019423 | Common:1; Rare:61 | ||||
chr14:74084355-74084619 | Common:2; Rare:78 | ||||
chr14:74292284-74292595 | Common:5; Rare:89; Clinvar:2; Clinvar (benign):7 | ||||
chr14:74302874-74303069 | Common:1; Rare:94; Clinvar (benign):3 | ||||
chr14:74348226-74348650 | Common:1; Rare:93 | ||||
chr14:74493439-74493781 | Common:3; Rare:116; Clinvar (benign):4 | ||||
chr14:74494031-74494319 | Rare:106; Clinvar (benign):2 | ||||
chr14:74713019-74713257 | Common:1; Rare:128 | ||||
chr14:74763089-74763397 | Rare:93 | ||||
chr14:74881813-74881990 | Rare:81 | ||||
chr14:74955594-74955743 | Common:1; Rare:31 | ||||
chr14:75051389-75051539 | Common:2; Rare:44; Clinvar:3; Clinvar (benign):2 |