Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1032436-1032669 | Common:1; Rare:70 | ||||
chr19:1085545-1085789 | Common:2; Rare:154 | ||||
chr19:1440410-1440570 | Rare:50 | ||||
chr19:1876123-1876283 | Common:1; Rare:65 | ||||
chr19:2115219-2115562 | Common:4; Rare:129 | ||||
chr19:2185828-2185863 | Rare:9 | ||||
chr19:2462091-2462273 | Rare:34 | ||||
chr19:2540032-2540228 | Common:1; Rare:37 | ||||
chr19:2543617-2543726 | Common:3; Rare:18 | ||||
chr19:2737917-2738206 | Rare:52 | ||||
chr19:3000659-3000804 | Common:1; Rare:52 | ||||
chr19:3980514-3980922 | Common:1; Rare:148; Clinvar:3; Clinvar (benign):2 | ||||
chr19:4035887-4035933 | Common:7; Rare:6 | ||||
chr19:4433637-4433882 | Rare:45 | ||||
chr19:4493736-4494012 | Common:1; Rare:96 |