Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47256438-47256583 | Rare:53 | ||||
chr19:47484261-47484317 | Rare:14 | ||||
chr19:47778413-47778772 | Common:2; Rare:123 | ||||
chr19:48170266-48170709 | Common:2; Rare:120 | ||||
chr19:48445881-48446005 | Rare:45 | ||||
chr19:48619139-48619537 | Common:1; Rare:134 | ||||
chr19:48624093-48624415 | Common:1; Rare:84 | ||||
chr19:48753669-48753793 | Common:1; Rare:34 | ||||
chr19:48811006-48811137 | Rare:44 | ||||
chr19:48868574-48868936 | Common:2; Rare:70 | ||||
chr19:48965398-48965609 | Rare:65; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:48993285-48993533 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
chr19:49085109-49085492 | Common:3; Rare:153 | ||||
chr19:49155394-49155529 | Rare:24 | ||||
chr19:49335301-49335446 | Rare:25 |