Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174799569-174799779 | Rare:43 | ||||
chr1:174964630-174964833 | Rare:37 | ||||
chr1:174999615-175000183 | Common:3; Rare:193 | ||||
chr1:175023404-175023691 | Common:1; Rare:83 | ||||
chr1:176207251-176207344 | Common:1; Rare:48 | ||||
chr1:178724902-178725359 | Common:12; Rare:144 | ||||
chr1:178869239-178869341 | Common:1; Rare:13 | ||||
chr1:178871003-178871114 | Rare:17 | ||||
chr1:178871159-178871237 | Rare:21 | ||||
chr1:179293667-179293855 | Common:2; Rare:65 | ||||
chr1:179365676-179365978 | Common:6; Rare:77 | ||||
chr1:179882151-179882313 | Common:1; Rare:31 | ||||
chr1:179882493-179882957 | Common:1; Rare:234; Clinvar:10; Clinvar (benign):4 | ||||
chr1:179954675-179954814 | Common:1; Rare:33 | ||||
chr1:180631892-180632135 | Common:3; Rare:91 |