Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149636682-149636766 | Common:4; Rare:24 | ||||
chr1:150561340-150561625 | Common:1; Rare:74 | ||||
chr1:151058592-151058870 | Common:1; Rare:42 | ||||
chr1:151945756-151946020 | Common:3; Rare:57 | ||||
chr1:153543045-153543219 | Common:3; Rare:34 | ||||
chr1:154326402-154326438 | Rare:5 | ||||
chr1:155194704-155194754 | Common:1; Rare:16 | ||||
chr1:156130308-156130688 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:156502901-156503134 | Common:1; Rare:41 | ||||
chr1:156748909-156749053 | Common:1; Rare:25 | ||||
chr1:159910552-159910732 | Rare:32 | ||||
chr1:161530931-161531107 | Common:4; Rare:70 | ||||
chr1:161612458-161612712 | Common:6; Rare:100 | ||||
chr1:164711623-164711817 | Rare:35 | ||||
chr1:165896164-165896198 | Rare:4 |