Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10333517-10333709 | Rare:64 | ||||
chr19:11089322-11089473 | Rare:23; Clinvar:7; Clinvar (pathogenic):1 | ||||
chr19:11197504-11197600 | Rare:25 | ||||
chr19:11559201-11559399 | Common:1; Rare:58 | ||||
chr19:12551483-12551706 | Common:2; Rare:54 | ||||
chr19:12610711-12610941 | Rare:76 | ||||
chr19:12681821-12682058 | Common:4; Rare:97 | ||||
chr19:12881460-12881596 | Rare:24 | ||||
chr19:13150216-13150457 | Common:1; Rare:82 | ||||
chr19:13731640-13731781 | Common:4; Rare:31 | ||||
chr19:14419287-14419615 | Common:1; Rare:78 | ||||
chr19:14529252-14529633 | Common:1; Rare:150 | ||||
chr19:16197783-16197989 | Common:2; Rare:76 | ||||
chr19:17215335-17215411 | Rare:33 | ||||
chr19:17405585-17405714 | Common:1; Rare:23 |