Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73950062-73950330 | Common:6; Rare:115; Clinvar (benign):4 | ||||
chr14:74019286-74019436 | Common:1; Rare:55 | ||||
chr14:74084399-74084547 | Common:1; Rare:46 | ||||
chr14:74302910-74303040 | Common:1; Rare:63; Clinvar (benign):1 | ||||
chr14:74493371-74493777 | Common:4; Rare:123; Clinvar (benign):4 | ||||
chr14:74713042-74713200 | Rare:91 | ||||
chr14:75002741-75002947 | Common:1; Rare:59; Clinvar:2 | ||||
chr14:75069556-75069680 | Common:1; Rare:21 | ||||
chr14:75126985-75127087 | Rare:37 | ||||
chr14:75660800-75661003 | Rare:50 | ||||
chr14:75661161-75661330 | Common:2; Rare:45 | ||||
chr14:75985709-75985790 | Rare:36; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr14:76812874-76813035 | Common:1; Rare:52 | ||||
chr14:77097903-77098354 | Rare:145 | ||||
chr14:77141778-77141925 | Common:1; Rare:22 |