Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:124673712-124673940 | Common:4; Rare:67 | ||||
chr11:125111712-125111957 | Common:3; Rare:52 | ||||
chr11:125592520-125592913 | Common:6; Rare:128 | ||||
chr11:125887480-125887742 | Common:2; Rare:85 | ||||
chr11:126211624-126211806 | Rare:84 | ||||
chr11:126268556-126268624 | Common:2; Rare:17 | ||||
chr11:126268805-126269207 | Common:2; Rare:157; Clinvar:2; Clinvar (benign):4 | ||||
chr11:126355554-126355760 | Rare:53 | ||||
chr11:128693801-128694115 | Common:2; Rare:57 | ||||
chr11:130069279-130069466 | Common:1; Rare:35 | ||||
chr11:130069651-130069946 | Common:2; Rare:106 | ||||
chr11:134253306-134253584 | Common:2; Rare:89; Clinvar (benign):1 | ||||
chr12:991100-991254 | Common:1; Rare:58 | ||||
chr12:2004438-2004669 | Common:2; Rare:67 | ||||
chr12:2877045-2877277 | Rare:77 |