Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161132426-161132700 | Common:1; Rare:94 | ||||
chr1:161159392-161159532 | Common:1; Rare:40 | ||||
chr1:161166268-161166489 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161198994-161199326 | Rare:48 | ||||
chr1:161258501-161258747 | Common:1; Rare:54 | ||||
chr1:161314265-161314407 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:161766157-161766376 | Common:3; Rare:67 | ||||
chr1:162497756-162497859 | Common:1; Rare:34 | ||||
chr1:162561375-162561672 | Common:3; Rare:113 | ||||
chr1:162790545-162790779 | Common:4; Rare:66 | ||||
chr1:163202904-163203223 | Common:1; Rare:60 | ||||
chr1:163321727-163321958 | Common:1; Rare:62 | ||||
chr1:164558873-164559184 | Common:1; Rare:87 | ||||
chr1:165698493-165698757 | Common:5; Rare:105 | ||||
chr1:165768760-165769039 | Common:2; Rare:111 |