Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40691504-40691843 | Common:2; Rare:158 | ||||
chr1:40979408-40979739 | Common:4; Rare:106 | ||||
chr1:42335199-42335304 | Common:1; Rare:46 | ||||
chr1:42456446-42456586 | Rare:62 | ||||
chr1:42766976-42767314 | Common:5; Rare:116; Clinvar (benign):1 | ||||
chr1:42816985-42817136 | Common:1; Rare:39 | ||||
chr1:42817225-42817512 | Rare:99 | ||||
chr1:42846407-42846638 | Common:1; Rare:62 | ||||
chr1:42958827-42959078 | Common:4; Rare:71; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43358863-43358986 | Rare:30 | ||||
chr1:43367993-43368178 | Rare:47 | ||||
chr1:43389752-43389914 | Common:3; Rare:68 | ||||
chr1:44674446-44674700 | Common:2; Rare:65 | ||||
chr1:44775480-44775599 | Rare:48 | ||||
chr1:44776561-44776771 | Rare:69 |