Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:45000733-45000968 | Common:1; Rare:102 | ||||
chr10:45374009-45374309 | Common:6; Rare:107 | ||||
chr10:45727116-45727315 | Common:3; Rare:78 | ||||
chr10:45972359-45972564 | Common:1; Rare:66 | ||||
chr10:46398289-46398424 | Common:3; Rare:57 | ||||
chr10:49941881-49942124 | Rare:73 | ||||
chr10:50067862-50067995 | Common:2; Rare:64 | ||||
chr10:50623864-50624084 | Common:1; Rare:84 | ||||
chr10:50624852-50624960 | Rare:41 | ||||
chr10:50991249-50991370 | Common:2; Rare:44 | ||||
chr10:51074391-51074575 | Common:1; Rare:41; Clinvar (benign):2 | ||||
chr10:51699557-51699649 | Common:1; Rare:32 | ||||
chr10:58268945-58269278 | Common:5; Rare:108 | ||||
chr10:59176476-59176619 | Common:4; Rare:43 | ||||
chr10:60300531-60300604 | Rare:15 |