Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:54115265-54115425 | Common:1; Rare:38; Clinvar (benign):1 | ||||
chr19:54115613-54115797 | Common:2; Rare:47; Clinvar:5 | ||||
chr19:54189305-54189421 | Common:1; Rare:33 | ||||
chr19:54200680-54200906 | Common:4; Rare:89 | ||||
chr19:54449039-54449249 | Common:2; Rare:60 | ||||
chr19:55339561-55339915 | Common:1; Rare:93 | ||||
chr19:55385737-55385982 | Common:6; Rare:84 | ||||
chr19:55461595-55462004 | Common:5; Rare:118 | ||||
chr19:55599488-55599740 | Common:2; Rare:82 | ||||
chr19:55600050-55600373 | Common:2; Rare:119 | ||||
chr19:55624566-55624644 | Common:1; Rare:31 | ||||
chr19:55643460-55643656 | Common:3; Rare:64 | ||||
chr19:55654851-55655147 | Rare:102 | ||||
chr19:56314810-56314930 | Common:1; Rare:37 | ||||
chr19:56368061-56368347 | Common:3; Rare:102 |