Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:11374889-11375239 | Common:1; Rare:108 | ||||
chr19:11418467-11418683 | Rare:56 | ||||
chr19:11419196-11419454 | Common:1; Rare:70 | ||||
chr19:11435150-11435705 | Common:7; Rare:169; Clinvar:2; Clinvar (benign):5 | ||||
chr19:11538588-11538907 | Common:3; Rare:70 | ||||
chr19:11539760-11540005 | Common:1; Rare:51 | ||||
chr19:11559195-11559425 | Common:2; Rare:74 | ||||
chr19:11738850-11739203 | Common:4; Rare:97 | ||||
chr19:11766889-11767175 | Common:1; Rare:73 | ||||
chr19:11814127-11814298 | Common:1; Rare:43 | ||||
chr19:11887682-11887866 | Common:1; Rare:52 | ||||
chr19:11964910-11965091 | Common:1; Rare:45 | ||||
chr19:12035643-12035825 | Common:1; Rare:66 | ||||
chr19:12052959-12053095 | Rare:34 | ||||
chr19:12156657-12156871 | Common:1; Rare:50 |