Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50719369-50719647 | Common:1; Rare:106 | ||||
chr17:51260352-51260576 | Common:3; Rare:98 | ||||
chr17:54968631-54968773 | Common:3; Rare:70 | ||||
chr17:56914005-56914180 | Common:1; Rare:45 | ||||
chr17:57850001-57850274 | Common:1; Rare:89 | ||||
chr17:58692361-58692628 | Common:2; Rare:104; Clinvar (benign):12 | ||||
chr17:59106727-59106999 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59619574-59619935 | Common:3; Rare:128 | ||||
chr17:59707397-59707700 | Common:3; Rare:85; Clinvar (benign):3 | ||||
chr17:59892933-59893137 | Rare:58 | ||||
chr17:59964719-59964821 | Common:2; Rare:45 | ||||
chr17:63773538-63773852 | Common:2; Rare:104 | ||||
chr17:63827051-63827464 | Common:5; Rare:111 | ||||
chr17:65056597-65056902 | Common:3; Rare:120 | ||||
chr17:67717647-67717959 | Common:2; Rare:103 |