Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42817198-42817381 | Rare:76 | ||||
chr1:42846392-42846657 | Common:1; Rare:76 | ||||
chr1:42958849-42959046 | Common:1; Rare:51; Clinvar:4; Clinvar (benign):2 | ||||
chr1:43367946-43368187 | Rare:60 | ||||
chr1:43389757-43389968 | Common:4; Rare:93; Clinvar:1 | ||||
chr1:43707346-43707658 | Common:2; Rare:88 | ||||
chr1:43946589-43946983 | Rare:104 | ||||
chr1:43974788-43975046 | Common:3; Rare:69 | ||||
chr1:44213330-44213504 | Common:1; Rare:35 | ||||
chr1:44674413-44674724 | Common:3; Rare:84 | ||||
chr1:44775469-44775614 | Common:1; Rare:59 | ||||
chr1:44775833-44776140 | Common:2; Rare:112 | ||||
chr1:44777611-44778129 | Common:2; Rare:130 | ||||
chr1:45340004-45340031 | Rare:4 | ||||
chr1:45340109-45340212 | Rare:47; Clinvar:1; Clinvar (benign):3 |