Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53889760-53889974 | Common:2; Rare:66 | ||||
chr1:53946260-53946476 | Rare:78 | ||||
chr1:54053184-54053360 | Rare:56 | ||||
chr1:54053378-54053637 | Common:6; Rare:81 | ||||
chr1:54199999-54200215 | Rare:51 | ||||
chr1:54887155-54887366 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
chr1:58546696-58546847 | Common:4; Rare:74 | ||||
chr1:58700059-58700174 | Common:4; Rare:45 | ||||
chr1:61725109-61725208 | Rare:45 | ||||
chr1:62688254-62688535 | Common:1; Rare:107; Clinvar:1 | ||||
chr1:62784050-62784174 | Rare:48 | ||||
chr1:63367317-63367668 | Common:1; Rare:94 | ||||
chr1:63523161-63523584 | Common:3; Rare:116 | ||||
chr1:66533403-66533652 | Common:2; Rare:38 | ||||
chr1:66533869-66534169 | Common:2; Rare:75 |