Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:52397755-52397912 | Common:4; Rare:51 | ||||
chr19:52638334-52638528 | Common:4; Rare:50 | ||||
chr19:52786756-52786939 | Common:8; Rare:50 | ||||
chr19:52962847-52963072 | Common:3; Rare:72 | ||||
chr19:53193328-53193490 | Common:1; Rare:35 | ||||
chr19:54102674-54102904 | Common:4; Rare:63 | ||||
chr19:54115253-54115455 | Common:1; Rare:54; Clinvar (benign):1 | ||||
chr19:54115628-54115797 | Common:1; Rare:43; Clinvar:4 | ||||
chr19:54159682-54160073 | Rare:135 | ||||
chr19:54200705-54200906 | Common:4; Rare:82 | ||||
chr19:54449030-54449224 | Common:2; Rare:54 | ||||
chr19:55370450-55370579 | Rare:23 | ||||
chr19:55385759-55385987 | Common:6; Rare:78 | ||||
chr19:56368261-56368364 | Common:2; Rare:34 | ||||
chr19:56393517-56393675 | Common:2; Rare:50 |