Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26473042-26473251 | Rare:109 | ||||
chr1:26545613-26545895 | Common:1; Rare:56 | ||||
chr1:26787877-26788201 | Common:3; Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890229-26890386 | Common:1; Rare:67 | ||||
chr1:26900428-26900481 | Rare:22 | ||||
chr1:26921507-26921837 | Common:3; Rare:100 | ||||
chr1:26993543-26993692 | Common:4; Rare:42 | ||||
chr1:27012841-27012976 | Common:2; Rare:47 | ||||
chr1:27322222-27322327 | Common:1; Rare:47 | ||||
chr1:27366912-27367154 | Common:1; Rare:52 | ||||
chr1:27374780-27375060 | Rare:48 | ||||
chr1:27392490-27392695 | Common:1; Rare:63 | ||||
chr1:27490033-27490363 | Rare:107 | ||||
chr1:27725758-27726067 | Common:4; Rare:88 | ||||
chr1:27772886-27773326 | Common:1; Rare:139 |