Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:8444694-8444992 | Common:4; Rare:120 | ||||
chr19:9621200-9621512 | Common:3; Rare:85 | ||||
chr19:9827817-9827963 | Common:1; Rare:55 | ||||
chr19:10333517-10333691 | Rare:62 | ||||
chr19:10403458-10403695 | Rare:110 | ||||
chr19:10653839-10653881 | Rare:17 | ||||
chr19:11197510-11197676 | Common:1; Rare:54 | ||||
chr19:11435540-11435666 | Common:3; Rare:46; Clinvar:1; Clinvar (benign):3 | ||||
chr19:11559195-11559397 | Common:1; Rare:61 | ||||
chr19:12610811-12610958 | Rare:57 | ||||
chr19:12666707-12666852 | Rare:56; Clinvar:2 | ||||
chr19:12696611-12696690 | Rare:37 | ||||
chr19:13150225-13150457 | Common:1; Rare:79 | ||||
chr19:13747670-13747942 | Common:1; Rare:106 | ||||
chr19:13764384-13764563 | Common:4; Rare:55 |