Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:177969875-177970117 | Common:1; Rare:49 | ||||
chr1:178093581-178093819 | Common:4; Rare:81 | ||||
chr1:178725007-178725359 | Common:10; Rare:117 | ||||
chr1:178871037-178871147 | Rare:17 | ||||
chr1:179081893-179082112 | Common:1; Rare:69 | ||||
chr1:179293590-179293849 | Common:2; Rare:95 | ||||
chr1:179882208-179882308 | Rare:19 | ||||
chr1:179882609-179882841 | Rare:113; Clinvar:6; Clinvar (benign):1 | ||||
chr1:179954675-179954853 | Common:1; Rare:40 | ||||
chr1:179955074-179955142 | Rare:14 | ||||
chr1:180631984-180632199 | Common:2; Rare:88 | ||||
chr1:181088447-181088728 | Rare:98 | ||||
chr1:182391316-182391477 | Rare:32 | ||||
chr1:182391749-182392015 | Common:2; Rare:89; Clinvar:4; Clinvar (benign):2 | ||||
chr1:182789678-182789778 | Common:1; Rare:31 |