Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10502627-10502923 | Rare:81 | ||||
chr19:10568961-10569116 | Common:2; Rare:44 | ||||
chr19:10625371-10625620 | Common:3; Rare:66 | ||||
chr19:10631629-10631942 | Common:2; Rare:108 | ||||
chr19:10653770-10653911 | Rare:56 | ||||
chr19:10836268-10836540 | Common:2; Rare:69 | ||||
chr19:10928527-10928802 | Common:2; Rare:76 | ||||
chr19:10960680-10961167 | Common:4; Rare:180; Clinvar (benign):2 | ||||
chr19:11089145-11089517 | Rare:57; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:11155772-11156016 | Common:2; Rare:59 | ||||
chr19:11197504-11197687 | Common:1; Rare:59 | ||||
chr19:11203335-11203618 | Rare:63 | ||||
chr19:11239370-11239650 | Common:3; Rare:78 | ||||
chr19:11339577-11339764 | Common:3; Rare:45 | ||||
chr19:11374578-11374734 | Common:1; Rare:53 |