Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44986483-44986802 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
chr1:45011245-45011459 | Common:1; Rare:56 | ||||
chr1:45011984-45012331 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45012723-45012823 | Common:1; Rare:22 | ||||
chr1:45306379-45306643 | Rare:57 | ||||
chr1:45326757-45326958 | Rare:49 | ||||
chr1:45327060-45327152 | Rare:19 | ||||
chr1:45339519-45339818 | Rare:62 | ||||
chr1:45339860-45340103 | Common:2; Rare:85; Clinvar (benign):1 | ||||
chr1:45340107-45340301 | Rare:85; Clinvar:14; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:45340324-45340447 | Common:2; Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
chr1:45491065-45491419 | Common:3; Rare:95 | ||||
chr1:45499840-45500411 | Common:2; Rare:139; Clinvar:6; Clinvar (pathogenic):4 | ||||
chr1:45521795-45522147 | Common:1; Rare:133 | ||||
chr1:45522283-45522321 | Common:1; Rare:6 |