Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45012852-45013003 | Rare:56 | ||||
chr1:45205847-45206137 | Common:1; Rare:101 | ||||
chr1:45206338-45206690 | Common:1; Rare:115 | ||||
chr1:45326777-45326943 | Rare:40 | ||||
chr1:45339704-45339775 | Rare:18 | ||||
chr1:45339803-45340372 | Common:2; Rare:206; Clinvar:15; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr1:45340383-45340582 | Common:1; Rare:48; Clinvar:1 | ||||
chr1:45340866-45341113 | Common:1; Rare:55 | ||||
chr1:45341540-45341573 | Rare:16; Clinvar (pathogenic):1 | ||||
chr1:45491030-45491450 | Common:3; Rare:110 | ||||
chr1:45499600-45499629 | Rare:10 | ||||
chr1:45499809-45499882 | Rare:13 | ||||
chr1:45499910-45500369 | Common:2; Rare:104; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521221-45521482 | Common:1; Rare:61 | ||||
chr1:45521652-45522185 | Common:2; Rare:182 |