Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174999325-175000183 | Common:5; Rare:268 | ||||
chr1:175023404-175023612 | Common:1; Rare:58 | ||||
chr1:177164477-177164648 | Rare:57 | ||||
chr1:177164663-177164764 | Rare:31 | ||||
chr1:178093610-178093813 | Common:3; Rare:65 | ||||
chr1:178456627-178456790 | Rare:47 | ||||
chr1:178725114-178725344 | Common:10; Rare:82 | ||||
chr1:178871059-178871174 | Rare:19 | ||||
chr1:179293658-179293878 | Common:3; Rare:73 | ||||
chr1:179877730-179877915 | Rare:39 | ||||
chr1:179882106-179882307 | Common:1; Rare:37 | ||||
chr1:179882488-179882912 | Rare:212; Clinvar:9; Clinvar (benign):2 | ||||
chr1:180502307-180502697 | Common:1; Rare:132 | ||||
chr1:180502824-180502940 | Rare:44 | ||||
chr1:180631971-180632218 | Common:2; Rare:95 |