Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161117955-161118146 | Rare:96 | ||||
chr1:161132426-161132862 | Common:2; Rare:139 | ||||
chr1:161166268-161166512 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161197112-161197428 | Common:3; Rare:59 | ||||
chr1:161199051-161199326 | Rare:43 | ||||
chr1:161215132-161215365 | Common:2; Rare:77 | ||||
chr1:161225768-161226072 | Common:10; Rare:44 | ||||
chr1:161314265-161314443 | Common:4; Rare:74; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:161549799-161549900 | Rare:34 | ||||
chr1:161766163-161766406 | Common:3; Rare:81 | ||||
chr1:162023632-162023956 | Common:1; Rare:93 | ||||
chr1:162497761-162497867 | Common:1; Rare:40 | ||||
chr1:162561375-162561696 | Common:3; Rare:121 | ||||
chr1:162631065-162631377 | Common:5; Rare:60 | ||||
chr1:162790516-162790793 | Common:4; Rare:80 |