Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155965094-155965329 | Common:1; Rare:40 | ||||
chr1:156008943-156009107 | Rare:27 | ||||
chr1:156130365-156130634 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
chr1:156661399-156661539 | Common:1; Rare:29 | ||||
chr1:156678103-156678203 | Common:1; Rare:19 | ||||
chr1:156701015-156701161 | Common:1; Rare:29 | ||||
chr1:156708075-156708329 | Rare:49 | ||||
chr1:158100126-158100403 | Rare:58 | ||||
chr1:160027788-160028009 | Common:2; Rare:29 | ||||
chr1:160028256-160028315 | Rare:9 | ||||
chr1:160215571-160215756 | Common:1; Rare:39 | ||||
chr1:169115041-169115232 | Common:6; Rare:35 | ||||
chr1:169127073-169127381 | Rare:63 | ||||
chr1:170674369-170674681 | Common:1; Rare:61 | ||||
chr1:170676254-170676372 | Common:2; Rare:22 |