Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45507228-45507768 | Common:1; Rare:144 | ||||
chr19:45584772-45584991 | Common:4; Rare:88; Clinvar:1; Clinvar (benign):4 | ||||
chr19:45639362-45639478 | Common:1; Rare:33 | ||||
chr19:45692365-45692695 | Common:1; Rare:76 | ||||
chr19:45730853-45731052 | Common:1; Rare:42 | ||||
chr19:46600913-46601434 | Common:6; Rare:179; Clinvar (benign):3 | ||||
chr19:47112151-47112388 | Rare:75 | ||||
chr19:47256472-47256577 | Rare:39 | ||||
chr19:47484250-47484300 | Rare:13 | ||||
chr19:47778400-47778788 | Common:3; Rare:133 | ||||
chr19:48170246-48170704 | Common:2; Rare:126 | ||||
chr19:48255573-48255743 | Common:1; Rare:30 | ||||
chr19:48255896-48255917 | Common:1; Rare:4 | ||||
chr19:48325258-48325591 | Common:2; Rare:74 | ||||
chr19:48390881-48390978 | Rare:9 |