Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:6707076-6707541 | Common:2; Rare:142; Clinvar:1; Clinvar (benign):4 | ||||
chr19:6745514-6745747 | Common:1; Rare:48 | ||||
chr19:8609548-8609845 | Common:1; Rare:63 | ||||
chr19:10812124-10812366 | Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr19:13835821-13835922 | Rare:22 | ||||
chr19:13839288-13839352 | Rare:10 | ||||
chr19:13840669-13840729 | Rare:8 | ||||
chr19:13840787-13840834 | Common:1; Rare:10 | ||||
chr19:14621999-14622327 | Common:1; Rare:17 | ||||
chr19:16070235-16070393 | Rare:36 | ||||
chr19:16078530-16078590 | Rare:16 | ||||
chr19:16078593-16078709 | Rare:19 | ||||
chr19:16283684-16283823 | Rare:31 | ||||
chr19:20423682-20423745 | Common:1; Rare:19 | ||||
chr19:27793350-27793475 | Common:2; Rare:33 |