Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:45727127-45727307 | Common:2; Rare:71 | ||||
chr10:45972349-45972587 | Common:1; Rare:76 | ||||
chr10:46030542-46030739 | Common:1; Rare:64 | ||||
chr10:46911377-46911461 | Rare:7 | ||||
chr10:48306394-48306731 | Common:2; Rare:136 | ||||
chr10:49188337-49188612 | Common:2; Rare:70 | ||||
chr10:49539014-49539361 | Common:4; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
chr10:49941928-49942124 | Rare:57 | ||||
chr10:50067837-50068008 | Common:4; Rare:79 | ||||
chr10:50623891-50624079 | Common:1; Rare:76 | ||||
chr10:50624873-50624969 | Common:1; Rare:38 | ||||
chr10:50739887-50739978 | Rare:19 | ||||
chr10:51074410-51074575 | Common:1; Rare:37; Clinvar (benign):2 | ||||
chr10:56361229-56361475 | Common:5; Rare:77 | ||||
chr10:58268943-58269231 | Common:5; Rare:85 |