Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43367993-43368235 | Rare:66 | ||||
chr1:43389765-43389940 | Common:3; Rare:74 | ||||
chr1:43946502-43946984 | Rare:132 | ||||
chr1:44213275-44213498 | Common:2; Rare:45 | ||||
chr1:44674401-44674724 | Common:3; Rare:89 | ||||
chr1:44739682-44739872 | Common:1; Rare:68 | ||||
chr1:44775462-44775599 | Rare:53 | ||||
chr1:44775833-44776140 | Common:2; Rare:112 | ||||
chr1:44986555-44986673 | Common:1; Rare:21 | ||||
chr1:45340388-45340502 | Common:1; Rare:30; Clinvar:1 | ||||
chr1:45500050-45500348 | Common:1; Rare:73; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521856-45521972 | Common:1; Rare:48 | ||||
chr1:45550741-45551098 | Common:3; Rare:85 | ||||
chr1:45583835-45584060 | Common:1; Rare:74 | ||||
chr1:45687054-45687289 | Common:1; Rare:68 |