Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:56913985-56914176 | Common:1; Rare:53 | ||||
chr17:57084971-57085105 | Rare:48 | ||||
chr17:57850002-57850279 | Common:1; Rare:91 | ||||
chr17:58692501-58692673 | Common:2; Rare:94; Clinvar:12; Clinvar (benign):20 | ||||
chr17:59106675-59106999 | Common:3; Rare:109; Clinvar:5; Clinvar (benign):4 | ||||
chr17:59155144-59155334 | Common:1; Rare:51 | ||||
chr17:59619569-59620081 | Common:3; Rare:176 | ||||
chr17:59707397-59707732 | Common:3; Rare:91; Clinvar (benign):3 | ||||
chr17:59837635-59838054 | Rare:63 | ||||
chr17:59892744-59893168 | Common:1; Rare:118 | ||||
chr17:59964775-59965096 | Rare:82 | ||||
chr17:60078913-60079058 | Common:5; Rare:58 | ||||
chr17:60526160-60526311 | Rare:61 | ||||
chr17:63550175-63550513 | Common:2; Rare:75 | ||||
chr17:63773462-63773800 | Common:2; Rare:109 |