Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49487366-49487644 | Common:4; Rare:103 | ||||
chr19:49580536-49580686 | Rare:47 | ||||
chr19:49665777-49666027 | Common:2; Rare:129; Clinvar (pathogenic):1 | ||||
chr19:49867538-49867643 | Common:2; Rare:35 | ||||
chr19:49928707-49928763 | Rare:13 | ||||
chr19:49929404-49929832 | Common:7; Rare:147 | ||||
chr19:50384288-50384371 | Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
chr19:50476346-50476536 | Rare:85 | ||||
chr19:50968106-50968272 | Common:2; Rare:47 | ||||
chr19:52269432-52269603 | Common:1; Rare:59 | ||||
chr19:52397755-52397879 | Common:2; Rare:36 | ||||
chr19:53254856-53255042 | Common:1; Rare:62 | ||||
chr19:53867583-53867941 | Common:1; Rare:88 | ||||
chr19:53869624-53869786 | Common:1; Rare:40 | ||||
chr19:54102684-54102894 | Common:3; Rare:55 |