Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:58692520-58692668 | Common:2; Rare:82; Clinvar:10; Clinvar (benign):20 | ||||
chr17:59106675-59106972 | Common:3; Rare:98; Clinvar:5; Clinvar (benign):4 | ||||
chr17:59155101-59155781 | Common:2; Rare:175 | ||||
chr17:59619557-59620031 | Common:3; Rare:162 | ||||
chr17:59620035-59620084 | Rare:16 | ||||
chr17:59707397-59707727 | Common:3; Rare:90; Clinvar (benign):3 | ||||
chr17:59837626-59837975 | Rare:49 | ||||
chr17:59892709-59893149 | Rare:117 | ||||
chr17:59964710-59964861 | Common:2; Rare:62 | ||||
chr17:60078904-60078974 | Common:4; Rare:37 | ||||
chr17:60526160-60526336 | Rare:77 | ||||
chr17:62423782-62423905 | Common:1; Rare:43 | ||||
chr17:63550160-63550669 | Common:3; Rare:114 | ||||
chr17:63600818-63600922 | Rare:29; Clinvar:2 | ||||
chr17:63700110-63700348 | Common:1; Rare:63 |