Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:3361182-3361358 | Common:1; Rare:43 | ||||
chr19:3785210-3785390 | Common:2; Rare:48 | ||||
chr19:3980514-3980883 | Common:1; Rare:138; Clinvar:2; Clinvar (benign):2 | ||||
chr19:5205878-5205968 | Rare:20 | ||||
chr19:5215327-5215587 | Common:3; Rare:81 | ||||
chr19:5287535-5287628 | Common:1; Rare:24 | ||||
chr19:7198052-7198294 | Common:4; Rare:77 | ||||
chr19:8370793-8370931 | Common:1; Rare:26 | ||||
chr19:14622070-14622327 | Common:1; Rare:16 | ||||
chr19:16078578-16078691 | Rare:17 | ||||
chr19:16078795-16078869 | Common:1; Rare:26 | ||||
chr19:16283573-16283820 | Common:1; Rare:57 | ||||
chr19:17580520-17580723 | Rare:56 | ||||
chr19:19776407-19776626 | Common:2; Rare:64 | ||||
chr19:20423677-20423769 | Common:1; Rare:25 |