Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47778434-47778748 | Common:2; Rare:103 | ||||
chr19:48110797-48110958 | Common:1; Rare:28 | ||||
chr19:48170270-48170709 | Common:2; Rare:118 | ||||
chr19:48445886-48446021 | Rare:49 | ||||
chr19:48469061-48469377 | Common:3; Rare:85 | ||||
chr19:48551985-48552191 | Common:1; Rare:47 | ||||
chr19:48619139-48619428 | Rare:92 | ||||
chr19:48624222-48624414 | Common:1; Rare:54 | ||||
chr19:48954644-48954922 | Common:1; Rare:100 | ||||
chr19:48993253-48993902 | Common:8; Rare:224; Clinvar:3; Clinvar (benign):2 | ||||
chr19:49085116-49085515 | Common:3; Rare:165 | ||||
chr19:49119112-49119373 | Rare:85 | ||||
chr19:49335362-49335454 | Common:1; Rare:22 | ||||
chr19:49362375-49362471 | Rare:25 | ||||
chr19:49513108-49513403 | Common:1; Rare:68 |