Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49453465-49453644 | Common:1; Rare:57 | ||||
chr19:49580528-49580686 | Rare:51 | ||||
chr19:49665709-49666027 | Common:3; Rare:147; Clinvar (pathogenic):1 | ||||
chr19:49867539-49867643 | Common:2; Rare:35 | ||||
chr19:49877572-49877717 | Common:1; Rare:42 | ||||
chr19:49877839-49878179 | Common:4; Rare:109 | ||||
chr19:49929074-49929219 | Common:3; Rare:46 | ||||
chr19:49929423-49929636 | Common:4; Rare:72 | ||||
chr19:50476384-50476539 | Rare:71 | ||||
chr19:51225056-51225124 | Rare:20 | ||||
chr19:51366333-51366571 | Common:7; Rare:66; Clinvar (benign):2 | ||||
chr19:51417543-51418018 | Common:2; Rare:91 | ||||
chr19:51927358-51927476 | Rare:36 | ||||
chr19:52008171-52008349 | Rare:49 | ||||
chr19:52028325-52028484 | Common:3; Rare:36 |