Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:50623872-50624079 | Common:1; Rare:82 | ||||
chr10:50624852-50624951 | Rare:38 | ||||
chr10:50990835-50990938 | Common:3; Rare:18 | ||||
chr10:50991207-50991381 | Common:4; Rare:53 | ||||
chr10:51074402-51074575 | Common:1; Rare:38; Clinvar (benign):2 | ||||
chr10:51699536-51699873 | Common:4; Rare:96 | ||||
chr10:58267886-58268245 | Common:1; Rare:95 | ||||
chr10:58268943-58269287 | Common:5; Rare:111 | ||||
chr10:58385294-58385528 | Common:2; Rare:84 | ||||
chr10:59362487-59362690 | Common:1; Rare:56 | ||||
chr10:60944682-60944925 | Common:2; Rare:54 | ||||
chr10:61453423-61453529 | Common:1; Rare:19 | ||||
chr10:61901562-61901729 | Common:1; Rare:43 | ||||
chr10:62048544-62048848 | Common:1; Rare:43 | ||||
chr10:62049036-62049101 | Rare:7 |