Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174799579-174799791 | Rare:46 | ||||
chr1:174999247-174999478 | Common:1; Rare:64 | ||||
chr1:174999574-175000183 | Common:3; Rare:206 | ||||
chr1:175023389-175023631 | Common:1; Rare:68 | ||||
chr1:176207226-176207345 | Common:1; Rare:61 | ||||
chr1:176207498-176207738 | Common:2; Rare:99 | ||||
chr1:178725039-178725340 | Common:10; Rare:106 | ||||
chr1:179081909-179081959 | Rare:16 | ||||
chr1:179293658-179293900 | Common:3; Rare:76 | ||||
chr1:179742754-179742910 | Common:1; Rare:22 | ||||
chr1:179743109-179743317 | Common:2; Rare:48 | ||||
chr1:179743363-179743530 | Common:3; Rare:44 | ||||
chr1:179877766-179877915 | Rare:30 | ||||
chr1:179882151-179882346 | Common:1; Rare:37 | ||||
chr1:179882460-179882928 | Rare:224; Clinvar:9; Clinvar (benign):2 |