Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:46495846-46496023 | Rare:53 | ||||
chr19:46600913-46601076 | Common:2; Rare:66 | ||||
chr19:46601147-46601437 | Common:4; Rare:85; Clinvar (benign):3 | ||||
chr19:46788587-46788623 | Rare:9 | ||||
chr19:47112146-47112339 | Rare:54 | ||||
chr19:47256472-47256577 | Rare:39 | ||||
chr19:47309686-47309867 | Rare:32 | ||||
chr19:47778386-47778772 | Common:2; Rare:135 | ||||
chr19:47780620-47780746 | Common:1; Rare:38 | ||||
chr19:48170266-48170704 | Common:2; Rare:119 | ||||
chr19:48390887-48390957 | Rare:6 | ||||
chr19:48445886-48446020 | Rare:48 | ||||
chr19:48619139-48619534 | Common:1; Rare:131 | ||||
chr19:48624057-48624438 | Common:1; Rare:93 | ||||
chr19:48646370-48646661 | Common:1; Rare:73 |