Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161166268-161166499 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161198975-161199304 | Rare:50 | ||||
chr1:161314321-161314412 | Common:2; Rare:38; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161549789-161549924 | Rare:47 | ||||
chr1:161766123-161766406 | Common:3; Rare:89 | ||||
chr1:162023632-162024027 | Common:1; Rare:123 | ||||
chr1:162561339-162561682 | Common:3; Rare:130 | ||||
chr1:162632256-162632568 | Rare:61 | ||||
chr1:162790542-162790781 | Common:4; Rare:69 | ||||
chr1:163321727-163322007 | Common:1; Rare:76 | ||||
chr1:164559613-164559727 | Common:2; Rare:26 | ||||
chr1:165630780-165630886 | Rare:40 | ||||
chr1:165698439-165698734 | Common:3; Rare:121 | ||||
chr1:165768690-165769019 | Common:2; Rare:121; Clinvar:1 | ||||
chr1:166839344-166839525 | Rare:54 |