Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44305001-44305141 | Rare:37 | ||||
chr19:44356681-44356817 | Common:1; Rare:21 | ||||
chr19:44500505-44500652 | Common:3; Rare:40 | ||||
chr19:45322790-45323129 | Common:3; Rare:65 | ||||
chr19:45406358-45406649 | Common:1; Rare:62 | ||||
chr19:45450751-45450999 | Common:4; Rare:46 | ||||
chr19:45507228-45507516 | Common:1; Rare:74 | ||||
chr19:45730890-45731084 | Common:1; Rare:43 | ||||
chr19:45777558-45777778 | Common:1; Rare:82; Clinvar (benign):1 | ||||
chr19:46346938-46347160 | Common:3; Rare:79 | ||||
chr19:46600913-46601402 | Common:5; Rare:165 | ||||
chr19:46745857-46746061 | Common:3; Rare:42 | ||||
chr19:47112154-47112333 | Rare:52 | ||||
chr19:47256472-47256568 | Rare:33 | ||||
chr19:47484182-47484300 | Common:2; Rare:38 |