Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73237409-73237556 | Common:1; Rare:32 | ||||
chr14:73851586-73851957 | Common:2; Rare:98 | ||||
chr14:73950113-73950317 | Common:5; Rare:74; Clinvar (benign):3 | ||||
chr14:74019263-74019436 | Common:1; Rare:68 | ||||
chr14:74302929-74303078 | Common:1; Rare:60; Clinvar (benign):1 | ||||
chr14:74493406-74493770 | Common:4; Rare:119; Clinvar (benign):4 | ||||
chr14:74713077-74713205 | Rare:62 | ||||
chr14:75002616-75003017 | Common:1; Rare:130; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr14:75126985-75127090 | Rare:37 | ||||
chr14:75660827-75660980 | Rare:40 | ||||
chr14:75661206-75661273 | Common:2; Rare:18 | ||||
chr14:77377055-77377410 | Common:2; Rare:102 | ||||
chr14:77457558-77457879 | Common:1; Rare:94 | ||||
chr14:77457987-77458117 | Rare:32 | ||||
chr14:77708003-77708113 | Rare:52 |