Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19370951-19371410 | Rare:131 | ||||
chr19:19776330-19776830 | Common:7; Rare:212 | ||||
chr19:23549502-23549823 | Common:7; Rare:109 | ||||
chr19:27793064-27793498 | Common:11; Rare:182 | ||||
chr19:27793663-27794068 | Common:1; Rare:133 | ||||
chr19:32373070-32373490 | Common:6; Rare:138 | ||||
chr19:33037277-33037436 | Common:2; Rare:55 | ||||
chr19:33249350-33249710 | Common:6; Rare:164 | ||||
chr19:33819960-33820250 | Rare:95 | ||||
chr19:34134403-34134636 | Common:6; Rare:146 | ||||
chr19:34173280-34173710 | Common:5; Rare:133 | ||||
chr19:34366140-34366430 | Rare:149 | ||||
chr19:34377201-34377820 | Common:10; Rare:182; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:35120390-35120780 | Common:1; Rare:117 | ||||
chr19:35716850-35717310 | Common:7; Rare:150 |