Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:264558-265007 | Common:4; Rare:175 | ||||
chr2:677314-677557 | Common:1; Rare:103 | ||||
chr2:1373662-1374121 | Common:4; Rare:109 | ||||
chr2:1413178-1413627 | Common:3; Rare:116; Clinvar (benign):1 | ||||
chr2:1744379-1744668 | Common:2; Rare:100 | ||||
chr2:3282518-3282728 | Rare:61 | ||||
chr2:3377774-3377953 | Rare:52 | ||||
chr2:3379608-3379813 | Common:2; Rare:82 | ||||
chr2:3459765-3459923 | Rare:40 | ||||
chr2:3519442-3519660 | Common:2; Rare:67 | ||||
chr2:3558251-3558688 | Common:6; Rare:161 | ||||
chr2:3575098-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
chr2:3595043-3595155 | Rare:36 | ||||
chr2:8679147-8679283 | Rare:60 | ||||
chr2:8837486-8837734 | Common:1; Rare:91 |