Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45468665-45469065 | Common:3; Rare:80 | ||||
chr19:45506814-45506955 | Common:1; Rare:44 | ||||
chr19:45692384-45692706 | Common:1; Rare:73 | ||||
chr19:46600941-46601425 | Common:6; Rare:163; Clinvar (benign):2 | ||||
chr19:47112150-47112476 | Rare:102 | ||||
chr19:47113724-47113899 | Common:1; Rare:44 | ||||
chr19:47231141-47231451 | Common:5; Rare:101 | ||||
chr19:47256471-47256603 | Rare:48 | ||||
chr19:47274227-47274473 | Common:4; Rare:69 | ||||
chr19:47484173-47484428 | Common:2; Rare:76 | ||||
chr19:47729554-47729659 | Rare:15 | ||||
chr19:47778420-47778795 | Common:3; Rare:132 | ||||
chr19:48170211-48170709 | Common:3; Rare:138 | ||||
chr19:48249533-48249909 | Rare:86 | ||||
chr19:48255579-48255732 | Common:1; Rare:26 |