Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45091579-45091829 | Common:2; Rare:63 | ||||
chr19:45092815-45092994 | Common:1; Rare:53 | ||||
chr19:45363465-45363775 | Common:2; Rare:93; Clinvar:1 | ||||
chr19:45370548-45370800 | Common:2; Rare:74 | ||||
chr19:45406363-45406649 | Common:1; Rare:62 | ||||
chr19:45423491-45423797 | Common:3; Rare:64; Clinvar (benign):1 | ||||
chr19:45450733-45451012 | Common:4; Rare:52 | ||||
chr19:45469143-45469476 | Common:2; Rare:107 | ||||
chr19:45496942-45497258 | Common:2; Rare:96 | ||||
chr19:45507228-45507488 | Common:1; Rare:65 | ||||
chr19:45667816-45668280 | Common:3; Rare:75 | ||||
chr19:45692381-45692722 | Common:1; Rare:81 | ||||
chr19:45730855-45731099 | Common:1; Rare:55 | ||||
chr19:45769232-45769570 | Common:1; Rare:151 | ||||
chr19:45862530-45862675 | Rare:37 |