Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49640102-49640503 | Common:1; Rare:121 | ||||
chr19:49665557-49666017 | Common:6; Rare:209; Clinvar (pathogenic):1 | ||||
chr19:49817359-49817632 | Common:3; Rare:61 | ||||
chr19:49851042-49851182 | Common:1; Rare:56 | ||||
chr19:49867499-49867643 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
chr19:49877309-49877720 | Common:1; Rare:104 | ||||
chr19:49878026-49878141 | Common:1; Rare:35 | ||||
chr19:49929404-49929768 | Common:7; Rare:121 | ||||
chr19:50025347-50025691 | Common:5; Rare:106 | ||||
chr19:50384022-50384377 | Common:2; Rare:150; Clinvar:1; Clinvar (benign):2 | ||||
chr19:50476419-50476542 | Rare:51 | ||||
chr19:50511087-50511585 | Common:4; Rare:160 | ||||
chr19:50723504-50723823 | Rare:81 | ||||
chr19:51366272-51366589 | Common:8; Rare:98; Clinvar (benign):2 | ||||
chr19:51372948-51373149 | Common:2; Rare:33 |