Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:49941929-49942091 | Rare:44 | ||||
chr10:50067786-50067986 | Common:4; Rare:85 | ||||
chr10:50623872-50624094 | Common:1; Rare:86 | ||||
chr10:51074402-51074575 | Common:1; Rare:38; Clinvar (benign):2 | ||||
chr10:51699557-51699743 | Common:2; Rare:54 | ||||
chr10:56361236-56361459 | Common:5; Rare:70 | ||||
chr10:58269115-58269217 | Common:2; Rare:37 | ||||
chr10:58385225-58385482 | Common:4; Rare:83 | ||||
chr10:59362500-59362698 | Common:1; Rare:54 | ||||
chr10:61901641-61901724 | Rare:24 | ||||
chr10:62816360-62816527 | Rare:28 | ||||
chr10:63133253-63133363 | Common:2; Rare:37 | ||||
chr10:63269135-63269388 | Common:2; Rare:52 | ||||
chr10:66925962-66926081 | Common:1; Rare:30 | ||||
chr10:68331887-68332111 | Common:2; Rare:93 |