Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45011223-45011469 | Common:2; Rare:64 | ||||
chr1:45011975-45012332 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45306379-45306636 | Rare:54 | ||||
chr1:45326718-45327066 | Rare:84 | ||||
chr1:45339518-45339797 | Rare:60 | ||||
chr1:45339834-45340595 | Common:4; Rare:254; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr1:45340866-45340999 | Rare:26 | ||||
chr1:45341059-45341113 | Common:1; Rare:13 | ||||
chr1:45490856-45490873 | Rare:2 | ||||
chr1:45491078-45491207 | Common:2; Rare:42 | ||||
chr1:45499851-45500398 | Common:2; Rare:129; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521642-45522227 | Common:2; Rare:192 | ||||
chr1:45550457-45550586 | Common:1; Rare:29 | ||||
chr1:45550600-45550947 | Common:2; Rare:82 | ||||
chr1:45550950-45551137 | Common:2; Rare:42 |