Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173824331-173824694 | Rare:72 | ||||
chr1:173867969-173868151 | Rare:72 | ||||
chr1:174159179-174159560 | Common:6; Rare:130 | ||||
chr1:174999328-174999471 | Rare:40 | ||||
chr1:174999621-175000151 | Common:3; Rare:172 | ||||
chr1:175023404-175023626 | Common:1; Rare:60 | ||||
chr1:178725114-178725340 | Common:10; Rare:82 | ||||
chr1:178871027-178871114 | Rare:12 | ||||
chr1:179882106-179882306 | Common:1; Rare:37 | ||||
chr1:179882475-179882853 | Rare:177; Clinvar:7; Clinvar (benign):2 | ||||
chr1:182391316-182391480 | Rare:33 | ||||
chr1:182789622-182789778 | Common:2; Rare:51 | ||||
chr1:183635619-183636063 | Common:2; Rare:122 | ||||
chr1:183804975-183805238 | Rare:68 | ||||
chr1:184051676-184051758 | Common:2; Rare:29 |