Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42766528-42766722 | Rare:51; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:42766983-42767323 | Common:5; Rare:116; Clinvar (benign):1 | ||||
chr1:42817004-42817136 | Common:1; Rare:32 | ||||
chr1:42846392-42846638 | Common:1; Rare:68 | ||||
chr1:42958849-42959078 | Common:2; Rare:61; Clinvar:5; Clinvar (benign):2 | ||||
chr1:43358674-43359006 | Common:7; Rare:103 | ||||
chr1:43367931-43368212 | Rare:71 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 | ||||
chr1:43946645-43946977 | Rare:90 | ||||
chr1:43974788-43975058 | Common:3; Rare:73 | ||||
chr1:44213274-44213498 | Common:2; Rare:46 | ||||
chr1:44355276-44355470 | Common:1; Rare:44 | ||||
chr1:44674421-44674744 | Common:3; Rare:83 | ||||
chr1:44739648-44739934 | Common:3; Rare:113 | ||||
chr1:44775473-44775599 | Rare:52 |