Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45038937-45039097 | Rare:55 | ||||
chr19:45079195-45079297 | Rare:28 | ||||
chr19:45370555-45370775 | Common:2; Rare:66 | ||||
chr19:45406356-45406682 | Common:2; Rare:80 | ||||
chr19:45423837-45424012 | Common:2; Rare:38 | ||||
chr19:45692381-45692695 | Common:1; Rare:71 | ||||
chr19:45730869-45731060 | Common:1; Rare:42 | ||||
chr19:46346938-46347135 | Common:3; Rare:60 | ||||
chr19:46600972-46601391 | Common:4; Rare:139 | ||||
chr19:47256472-47256568 | Rare:33 | ||||
chr19:48170266-48170664 | Common:2; Rare:113 | ||||
chr19:48619139-48619409 | Rare:90 | ||||
chr19:48624084-48624381 | Common:1; Rare:73 | ||||
chr19:48811010-48811107 | Rare:39 | ||||
chr19:48993296-48993576 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):1 |