Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:203330663-203330712 | Rare:6 | ||||
chr2:203551443-203551447 | Rare:2 | ||||
chr2:206085233-206085349 | Rare:43 | ||||
chr2:206087809-206088016 | Common:4; Rare:40 | ||||
chr2:206152422-206152726 | Common:2; Rare:88; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr2:206161248-206161371 | Rare:32 | ||||
chr2:207163586-207163639 | Rare:8 | ||||
chr2:207683730-207684036 | Common:2; Rare:51 | ||||
chr2:207753434-207753725 | Rare:80 | ||||
chr2:216191475-216191708 | Common:1; Rare:41 | ||||
chr2:218006855-218007011 | Common:2; Rare:27 | ||||
chr2:218234137-218234319 | Rare:28 | ||||
chr2:218250543-218250703 | Common:3; Rare:35 | ||||
chr2:222843035-222843206 | Rare:25 | ||||
chr2:222870549-222870684 | Common:1; Rare:28 |