Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45038946-45039097 | Rare:52 | ||||
chr19:45091600-45091788 | Common:1; Rare:49 | ||||
chr19:45370526-45370731 | Common:2; Rare:64; Clinvar:1 | ||||
chr19:45406339-45406682 | Common:2; Rare:85 | ||||
chr19:45423502-45423679 | Common:2; Rare:35; Clinvar (benign):1 | ||||
chr19:45423813-45423932 | Common:2; Rare:30 | ||||
chr19:45469262-45469472 | Rare:62 | ||||
chr19:45506527-45506640 | Common:1; Rare:39 | ||||
chr19:45506832-45506969 | Common:1; Rare:39 | ||||
chr19:45507225-45507527 | Common:1; Rare:83 | ||||
chr19:45692381-45692722 | Common:1; Rare:81 | ||||
chr19:45730862-45731052 | Common:1; Rare:39 | ||||
chr19:46346951-46347160 | Common:3; Rare:73 | ||||
chr19:46413515-46413743 | Common:1; Rare:76 | ||||
chr19:46601021-46601431 | Common:5; Rare:129; Clinvar (benign):3 |