Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45326759-45326924 | Rare:43 | ||||
chr1:45339949-45340069 | Common:1; Rare:44; Clinvar (benign):1 | ||||
chr1:45340114-45340212 | Rare:45; Clinvar:1; Clinvar (benign):3 | ||||
chr1:45340329-45340593 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
chr1:45500046-45500351 | Common:1; Rare:75; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521809-45522087 | Common:1; Rare:105 | ||||
chr1:45550730-45551153 | Common:3; Rare:98 | ||||
chr1:45583931-45584204 | Common:1; Rare:106 | ||||
chr1:45615027-45615471 | Common:3; Rare:130 | ||||
chr1:45686466-45686668 | Rare:73 | ||||
chr1:45687054-45687357 | Common:1; Rare:80 | ||||
chr1:45688049-45688243 | Common:1; Rare:54 | ||||
chr1:45750615-45750839 | Rare:81 | ||||
chr1:45803455-45803619 | Common:2; Rare:57 | ||||
chr1:46028636-46028855 | Rare:59 |