Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:43527173-43527335 | Common:4; Rare:61; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr19:43670126-43670365 | Common:2; Rare:61 | ||||
chr19:43754850-43755102 | Common:3; Rare:100 | ||||
chr19:44141507-44141565 | Rare:5 | ||||
chr19:45038941-45039094 | Rare:52 | ||||
chr19:45507219-45507508 | Common:1; Rare:76 | ||||
chr19:46600987-46601391 | Common:4; Rare:134 | ||||
chr19:47256439-47256555 | Rare:38 | ||||
chr19:47483971-47484300 | Common:2; Rare:119; Clinvar:2 | ||||
chr19:48619146-48619507 | Common:1; Rare:117 | ||||
chr19:48993296-48993566 | Common:2; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
chr19:49929408-49929594 | Common:4; Rare:66 | ||||
chr19:49929923-49930212 | Common:1; Rare:68 | ||||
chr19:50476238-50476542 | Rare:141 | ||||
chr19:50723232-50723383 | Common:2; Rare:35 |