Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:43746293-43746461 | Common:1; Rare:66 | ||||
chr15:44288409-44288776 | Common:39; Rare:222 | ||||
chr15:44536867-44537200 | Common:1; Rare:118 | ||||
chr15:45587325-45587649 | Rare:108; Clinvar:3; Clinvar (benign):2 | ||||
chr15:48645657-48646132 | Common:3; Rare:150; Clinvar (benign):1 | ||||
chr15:49155565-49155819 | Common:2; Rare:86 | ||||
chr15:49423108-49423406 | Common:1; Rare:49 | ||||
chr15:49620760-49621093 | Common:6; Rare:126 | ||||
chr15:50354877-50354998 | Rare:18 | ||||
chr15:50355116-50355493 | Common:3; Rare:150 | ||||
chr15:50908597-50908760 | Common:1; Rare:68; Clinvar (benign):2 | ||||
chr15:52179921-52179999 | Common:1; Rare:30 | ||||
chr15:52679363-52679482 | Common:1; Rare:41 | ||||
chr15:55318886-55318985 | Common:1; Rare:30 | ||||
chr15:55319087-55319254 | Common:2; Rare:47 |