Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:48544558-48544632 | Rare:30 | ||||
chr17:48544693-48544778 | Common:2; Rare:26 | ||||
chr17:48545086-48545227 | Rare:24 | ||||
chr17:49677952-49678132 | Rare:44 | ||||
chr17:49788567-49788702 | Rare:37 | ||||
chr17:50345904-50346135 | Common:4; Rare:79 | ||||
chr17:50373137-50373229 | Common:2; Rare:49 | ||||
chr17:50478747-50478887 | Common:2; Rare:44 | ||||
chr17:51166664-51166954 | Rare:84 | ||||
chr17:51260370-51260581 | Common:3; Rare:97 | ||||
chr17:54968608-54968792 | Common:3; Rare:89 | ||||
chr17:58007216-58007560 | Common:1; Rare:123 | ||||
chr17:59155163-59155428 | Common:2; Rare:66 | ||||
chr17:59707377-59707742 | Common:4; Rare:101; Clinvar (benign):6 | ||||
chr17:59892930-59893137 | Rare:58 |