Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:70205659-70205774 | Common:3; Rare:48; Clinvar (benign):2 | ||||
chr19:571724-571793 | Common:2; Rare:14 | ||||
chr19:572237-572612 | Common:3; Rare:181 | ||||
chr19:663153-663445 | Common:2; Rare:118 | ||||
chr19:1438213-1438450 | Common:1; Rare:87 | ||||
chr19:2328559-2328677 | Rare:58 | ||||
chr19:2427539-2427676 | Common:1; Rare:62 | ||||
chr19:5622756-5623139 | Common:5; Rare:137 | ||||
chr19:5978078-5978393 | Common:3; Rare:117 | ||||
chr19:6393119-6393227 | Common:2; Rare:25 | ||||
chr19:7069647-7069710 | Rare:19 | ||||
chr19:7629538-7629848 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7943644-7943988 | Rare:90 | ||||
chr19:8321315-8321702 | Common:2; Rare:156 | ||||
chr19:8390055-8390384 | Common:1; Rare:87 |