Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160711757-160711978 | Common:3; Rare:53 | ||||
chr1:160795994-160796258 | Common:2; Rare:66 | ||||
chr1:161021111-161021260 | Common:1; Rare:43 | ||||
chr1:161038738-161038831 | Common:2; Rare:23 | ||||
chr1:161038903-161039072 | Common:2; Rare:55 | ||||
chr1:161045866-161046064 | Common:1; Rare:51 | ||||
chr1:161069877-161070124 | Rare:32 | ||||
chr1:161118012-161118137 | Rare:59 | ||||
chr1:161132583-161132669 | Common:1; Rare:34 | ||||
chr1:161159392-161159507 | Common:1; Rare:29 | ||||
chr1:161166257-161166480 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161225741-161226063 | Common:10; Rare:48 | ||||
chr1:161314262-161314404 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr1:161707063-161707267 | Common:3; Rare:50 | ||||
chr1:162497707-162497864 | Common:2; Rare:48 |