Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161153356-161153461 | Common:2; Rare:19 | ||||
chr1:161153662-161154501 | Common:3; Rare:210; Clinvar (pathogenic):1 | ||||
chr1:161159114-161159222 | Common:2; Rare:23 | ||||
chr1:161159321-161159619 | Common:2; Rare:95 | ||||
chr1:161159811-161160013 | Common:2; Rare:47 | ||||
chr1:161165686-161166037 | Common:2; Rare:81 | ||||
chr1:161166040-161166627 | Common:4; Rare:141; Clinvar:5; Clinvar (benign):2 | ||||
chr1:161166722-161166791 | Rare:7 | ||||
chr1:161166798-161166874 | Rare:30; Clinvar:2 | ||||
chr1:161166999-161167174 | Common:1; Rare:54 | ||||
chr1:161176566-161176874 | Rare:71 | ||||
chr1:161177031-161177171 | Common:1; Rare:41 | ||||
chr1:161177229-161177275 | Rare:15 | ||||
chr1:161177347-161177687 | Common:1; Rare:96 | ||||
chr1:161177717-161177829 | Rare:14 |