Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49362380-49362487 | Rare:33 | ||||
chr19:49453094-49453300 | Common:1; Rare:65 | ||||
chr19:49487342-49487675 | Common:5; Rare:133 | ||||
chr19:49527848-49528031 | Common:3; Rare:59 | ||||
chr19:49580515-49580650 | Rare:49 | ||||
chr19:49641812-49642237 | Rare:118 | ||||
chr19:49665611-49666020 | Common:6; Rare:191; Clinvar (pathogenic):1 | ||||
chr19:49690973-49691140 | Rare:37 | ||||
chr19:49808816-49808997 | Common:1; Rare:59 | ||||
chr19:49813202-49813350 | Rare:61 | ||||
chr19:49851058-49851120 | Rare:24 | ||||
chr19:49857463-49857775 | Common:3; Rare:112 | ||||
chr19:49867518-49867643 | Common:2; Rare:41; Clinvar:1 | ||||
chr19:49877293-49877724 | Common:1; Rare:112 | ||||
chr19:49877899-49878170 | Common:2; Rare:90 |