Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:46600956-46601409 | Common:5; Rare:153; Clinvar (benign):1 | ||||
chr19:46745835-46746066 | Common:3; Rare:46 | ||||
chr19:46746428-46746530 | Common:2; Rare:44 | ||||
chr19:46787260-46787397 | Common:1; Rare:32 | ||||
chr19:46787420-46787477 | Rare:17 | ||||
chr19:46787486-46787548 | Rare:19 | ||||
chr19:47231175-47231451 | Common:4; Rare:90 | ||||
chr19:47256459-47256580 | Rare:47 | ||||
chr19:47484173-47484295 | Common:2; Rare:40 | ||||
chr19:48170241-48170713 | Common:3; Rare:131 | ||||
chr19:48445912-48446003 | Rare:38 | ||||
chr19:48619141-48619657 | Common:1; Rare:165 | ||||
chr19:48624228-48624391 | Common:1; Rare:46 | ||||
chr19:48811004-48811126 | Rare:43 | ||||
chr19:48836471-48836585 | Rare:15 |