Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10653839-10653875 | Rare:15 | ||||
chr19:11089256-11089516 | Rare:42; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:11197509-11197622 | Common:1; Rare:30 | ||||
chr19:11559210-11559391 | Common:1; Rare:55 | ||||
chr19:11738922-11739233 | Common:3; Rare:82 | ||||
chr19:12035661-12035873 | Common:1; Rare:75 | ||||
chr19:12551452-12551676 | Common:2; Rare:59 | ||||
chr19:12610811-12610989 | Rare:65 | ||||
chr19:12666704-12666854 | Rare:58; Clinvar:2 | ||||
chr19:12791341-12791490 | Rare:33 | ||||
chr19:12792232-12792366 | Common:2; Rare:33 | ||||
chr19:12792547-12792774 | Common:1; Rare:30 | ||||
chr19:12938318-12938629 | Common:5; Rare:116 | ||||
chr19:13150236-13150439 | Common:1; Rare:71 | ||||
chr19:13731648-13731807 | Common:3; Rare:41 |