Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:38010643-38010720 | Rare:39 | ||||
chr10:42782691-42782825 | Rare:33 | ||||
chr10:43409152-43409450 | Common:3; Rare:98 | ||||
chr10:44959636-44959780 | Common:1; Rare:48 | ||||
chr10:45000850-45000961 | Common:1; Rare:40 | ||||
chr10:45727149-45727307 | Common:1; Rare:66 | ||||
chr10:45972398-45972554 | Rare:49 | ||||
chr10:48605086-48605225 | Common:1; Rare:41 | ||||
chr10:49539023-49539381 | Common:4; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
chr10:49941913-49942091 | Rare:51 | ||||
chr10:50067850-50067995 | Common:3; Rare:67 | ||||
chr10:50739890-50739962 | Rare:16 | ||||
chr10:58268937-58269268 | Common:6; Rare:103 | ||||
chr10:60300439-60300787 | Common:1; Rare:61 | ||||
chr10:62049189-62049481 | Common:2; Rare:67 |