Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50186315-50186690 | Common:2; Rare:99; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:50373168-50373246 | Common:3; Rare:31 | ||||
chr17:50719444-50719654 | Common:1; Rare:82 | ||||
chr17:50866343-50866575 | Common:3; Rare:72 | ||||
chr17:51153293-51153623 | Common:1; Rare:86 | ||||
chr17:51166251-51166505 | Common:2; Rare:57 | ||||
chr17:51260385-51260581 | Common:3; Rare:96 | ||||
chr17:54968631-54968792 | Common:3; Rare:77 | ||||
chr17:56914029-56914201 | Rare:45 | ||||
chr17:56978014-56978157 | Common:2; Rare:74 | ||||
chr17:57084980-57085081 | Rare:32 | ||||
chr17:57850006-57850274 | Common:1; Rare:86 | ||||
chr17:58352135-58352495 | Common:6; Rare:136 | ||||
chr17:59106707-59106930 | Common:2; Rare:70; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155146-59155545 | Common:2; Rare:92 |