Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:55269176-55269411 | Common:3; Rare:61 | ||||
chr2:55519423-55519757 | Common:1; Rare:93 | ||||
chr2:58241316-58241395 | Rare:49; Clinvar:3; Clinvar (benign):1 | ||||
chr2:61017434-61017762 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
chr2:61144916-61145165 | Common:3; Rare:83 | ||||
chr2:61888470-61888700 | Common:1; Rare:101 | ||||
chr2:63588412-63589025 | Common:2; Rare:176; Clinvar:2; Clinvar (benign):1 | ||||
chr2:63840822-63841154 | Common:2; Rare:91 | ||||
chr2:63841673-63841906 | Common:1; Rare:84 | ||||
chr2:64653868-64654148 | Common:2; Rare:117 | ||||
chr2:64989101-64989399 | Common:6; Rare:82 | ||||
chr2:65227603-65227897 | Rare:84 | ||||
chr2:66434956-66435171 | Common:1; Rare:49 | ||||
chr2:68157478-68157949 | Common:2; Rare:244 | ||||
chr2:68319396-68319687 | Common:2; Rare:87 |