Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:123633607-123633868 | Common:2; Rare:129; Clinvar:8; Clinvar (benign):1 | ||||
chr13:21176462-21176704 | Common:2; Rare:107 | ||||
chr13:23889434-23889545 | Common:1; Rare:39 | ||||
chr13:24512739-24512854 | Common:3; Rare:34 | ||||
chr13:26221798-26221924 | Rare:34 | ||||
chr13:26222259-26222375 | Common:2; Rare:33 | ||||
chr13:27251258-27251606 | Common:3; Rare:101 | ||||
chr13:30465828-30466117 | Common:1; Rare:88 | ||||
chr13:32315405-32315525 | Common:1; Rare:30; Clinvar:1 | ||||
chr13:33285677-33285913 | Rare:54 | ||||
chr13:36999303-36999457 | Rare:58 | ||||
chr13:37000757-37000800 | Rare:22 | ||||
chr13:41061356-41061579 | Common:2; Rare:64 | ||||
chr13:44989449-44989585 | Rare:50 | ||||
chr13:45120180-45120570 | Common:2; Rare:95 |