Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:59155557-59155784 | Rare:63 | ||||
chr17:59619569-59620010 | Common:3; Rare:157 | ||||
chr17:59707397-59707727 | Common:3; Rare:90; Clinvar (benign):3 | ||||
chr17:59837635-59838002 | Rare:57 | ||||
chr17:59892705-59893149 | Rare:118 | ||||
chr17:60078891-60079005 | Common:4; Rare:52 | ||||
chr17:60525939-60526338 | Common:1; Rare:141 | ||||
chr17:62423782-62423897 | Common:1; Rare:42 | ||||
chr17:63600773-63600927 | Rare:40; Clinvar:2 | ||||
chr17:63741775-63742042 | Common:3; Rare:110 | ||||
chr17:63773517-63773800 | Common:2; Rare:91 | ||||
chr17:63774083-63774268 | Common:8; Rare:98 | ||||
chr17:63827057-63827493 | Common:5; Rare:125 | ||||
chr17:64448784-64449163 | Common:2; Rare:45 | ||||
chr17:64497017-64497163 | Common:2; Rare:70; Clinvar:3; Clinvar (benign):2 |