Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43946574-43947004 | Rare:119 | ||||
chr1:43974771-43975026 | Common:3; Rare:70 | ||||
chr1:44674413-44674744 | Common:3; Rare:88 | ||||
chr1:44739674-44739897 | Common:1; Rare:88 | ||||
chr1:44775426-44775607 | Common:1; Rare:71 | ||||
chr1:44775841-44776140 | Common:2; Rare:108 | ||||
chr1:44986532-44986671 | Common:2; Rare:29; Clinvar (benign):1 | ||||
chr1:45339996-45340041 | Rare:12 | ||||
chr1:45340114-45340178 | Rare:23 | ||||
chr1:45340388-45340465 | Common:1; Rare:18; Clinvar:1 | ||||
chr1:45491108-45491429 | Common:3; Rare:83 | ||||
chr1:45500056-45500361 | Common:1; Rare:74; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521818-45522093 | Common:1; Rare:101 | ||||
chr1:45550552-45551133 | Common:4; Rare:133 | ||||
chr1:45583927-45584089 | Rare:64 |