Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44259832-44259921 | Common:1; Rare:24 | ||||
chr19:44304992-44305112 | Rare:35 | ||||
chr19:44356672-44356821 | Common:1; Rare:26 | ||||
chr19:44808939-44809105 | Rare:53 | ||||
chr19:44954910-44955010 | Common:2; Rare:27 | ||||
chr19:45079173-45079317 | Rare:38 | ||||
chr19:45406355-45406663 | Common:1; Rare:72 | ||||
chr19:45692372-45692713 | Common:1; Rare:79 | ||||
chr19:46600984-46601416 | Common:4; Rare:149; Clinvar (benign):1 | ||||
chr19:46787262-46787590 | Common:1; Rare:85 | ||||
chr19:46788573-46788864 | Common:2; Rare:66 | ||||
chr19:47232680-47232822 | Rare:27 | ||||
chr19:47256451-47256568 | Rare:41 | ||||
chr19:47484169-47484381 | Common:2; Rare:69 | ||||
chr19:47778411-47778803 | Common:3; Rare:135 |