Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41350719-41351011 | Common:2; Rare:61 | ||||
chr19:41353881-41354172 | Rare:84 | ||||
chr19:41397320-41397509 | Common:3; Rare:51 | ||||
chr19:41627018-41627226 | Common:1; Rare:44 | ||||
chr19:41860011-41860506 | Common:5; Rare:178; Clinvar:4; Clinvar (benign):4 | ||||
chr19:41956905-41957076 | Rare:55 | ||||
chr19:42070178-42070312 | Rare:32 | ||||
chr19:42075786-42076303 | Common:4; Rare:142 | ||||
chr19:42132402-42132645 | Rare:49 | ||||
chr19:42217751-42218053 | Common:2; Rare:93 | ||||
chr19:42220112-42220345 | Common:2; Rare:66 | ||||
chr19:42255127-42255347 | Common:1; Rare:75 | ||||
chr19:42268232-42268581 | Rare:73 | ||||
chr19:42302282-42302722 | Rare:118 | ||||
chr19:43504089-43504363 | Common:6; Rare:87 |