Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48445768-48446079 | Common:2; Rare:109 | ||||
chr19:48469079-48469409 | Common:3; Rare:95 | ||||
chr19:48619125-48619654 | Common:1; Rare:171 | ||||
chr19:48624201-48624451 | Common:1; Rare:72 | ||||
chr19:48637349-48637718 | Common:1; Rare:90 | ||||
chr19:48810849-48811128 | Rare:87 | ||||
chr19:48835818-48835970 | Common:1; Rare:48 | ||||
chr19:48900133-48900407 | Common:1; Rare:85 | ||||
chr19:48918725-48919080 | Common:3; Rare:120 | ||||
chr19:48965219-48965926 | Common:1; Rare:241; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
chr19:48993245-48993576 | Common:3; Rare:147; Clinvar:3; Clinvar (benign):2 | ||||
chr19:48993757-48993915 | Common:4; Rare:52 | ||||
chr19:49085100-49085582 | Common:3; Rare:187 | ||||
chr19:49114319-49114615 | Common:4; Rare:82 | ||||
chr19:49115013-49115304 | Common:1; Rare:68 |