Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:51153000-51153245 | Rare:41; Clinvar:3; Clinvar (benign):3 | ||||
chr10:56361211-56361490 | Common:6; Rare:98 | ||||
chr10:58268932-58269231 | Common:6; Rare:87 | ||||
chr10:58512706-58512919 | Common:1; Rare:95 | ||||
chr10:61901197-61901315 | Common:1; Rare:26 | ||||
chr10:63521817-63521947 | Common:4; Rare:52 | ||||
chr10:68332844-68333044 | Common:1; Rare:55 | ||||
chr10:68527399-68527575 | Common:2; Rare:59 | ||||
chr10:68913229-68913462 | Rare:65 | ||||
chr10:69801624-69801987 | Common:2; Rare:93 | ||||
chr10:70163502-70163803 | Common:4; Rare:57 | ||||
chr10:71819465-71819895 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):4 | ||||
chr10:72216244-72216507 | Common:2; Rare:77 | ||||
chr10:73110186-73110507 | Rare:55 | ||||
chr10:73167965-73168187 | Rare:63 |