Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45011980-45012295 | Common:3; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45012656-45012807 | Common:1; Rare:23 | ||||
chr1:45205863-45206163 | Common:1; Rare:105 | ||||
chr1:45206347-45206375 | Rare:8 | ||||
chr1:45206513-45206685 | Rare:49 | ||||
chr1:45326777-45327024 | Rare:52 | ||||
chr1:45339518-45340360 | Common:2; Rare:264; Clinvar:15; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr1:45340367-45340622 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr1:45340860-45340968 | Rare:21 | ||||
chr1:45491097-45491437 | Common:3; Rare:87 | ||||
chr1:45499937-45500386 | Common:2; Rare:115; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45500525-45500557 | Rare:5 | ||||
chr1:45521214-45521444 | Rare:55 | ||||
chr1:45521677-45522292 | Common:3; Rare:198 | ||||
chr1:45550646-45550914 | Common:2; Rare:74 |