Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:229625950-229626277 | Rare:111 | ||||
chr1:230869001-230869073 | Common:1; Rare:12 | ||||
chr1:230978739-230979115 | Common:2; Rare:141 | ||||
chr1:231241101-231241269 | Rare:93; Clinvar:3 | ||||
chr1:231337819-231338056 | Common:2; Rare:86 | ||||
chr1:231528492-231528738 | Common:2; Rare:84 | ||||
chr1:234373387-234373554 | Common:1; Rare:86; Clinvar (benign):3 | ||||
chr1:234373642-234373768 | Rare:51; Clinvar (benign):3 | ||||
chr1:234608177-234608295 | Rare:39 | ||||
chr1:235328105-235328606 | Common:4; Rare:148 | ||||
chr1:235866858-235867128 | Common:3; Rare:81 | ||||
chr1:236064991-236065367 | Common:3; Rare:135; Clinvar (pathogenic):1 | ||||
chr1:236523882-236524036 | Common:2; Rare:42 | ||||
chr1:236604464-236604631 | Common:4; Rare:49 | ||||
chr1:239386480-239386712 | Rare:38 |