Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:34734118-34734285 | Common:1; Rare:56 | ||||
chr19:34773204-34773324 | Common:1; Rare:37 | ||||
chr19:34926826-34926939 | Common:1; Rare:43 | ||||
chr19:35154566-35154857 | Rare:52 | ||||
chr19:35328953-35329203 | Common:1; Rare:59 | ||||
chr19:35545454-35545686 | Common:4; Rare:78 | ||||
chr19:35628732-35629087 | Common:4; Rare:105 | ||||
chr19:35648107-35648385 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
chr19:35745397-35745700 | Rare:89 | ||||
chr19:35757855-35758204 | Common:2; Rare:103 | ||||
chr19:36014192-36014525 | Common:2; Rare:92 | ||||
chr19:36054230-36054526 | Common:3; Rare:91 | ||||
chr19:36114828-36114959 | Common:1; Rare:65 | ||||
chr19:36215068-36215179 | Rare:35 | ||||
chr19:36379163-36379312 | Common:2; Rare:66 |