Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:45645644-45645904 | Common:1; Rare:46 | ||||
chr15:48645698-48645893 | Common:2; Rare:64; Clinvar (benign):1 | ||||
chr15:48878034-48878203 | Rare:66 | ||||
chr15:49155538-49155838 | Common:2; Rare:99 | ||||
chr15:49423111-49423279 | Common:1; Rare:34 | ||||
chr15:49620816-49621103 | Common:6; Rare:110 | ||||
chr15:50355154-50355483 | Common:3; Rare:127 | ||||
chr15:50424126-50424466 | Common:2; Rare:123 | ||||
chr15:50686721-50686905 | Common:4; Rare:79 | ||||
chr15:50765569-50765777 | Common:2; Rare:71 | ||||
chr15:50908585-50908751 | Common:2; Rare:65; Clinvar (benign):2 | ||||
chr15:51971719-51971841 | Rare:57 | ||||
chr15:52019051-52019243 | Common:1; Rare:99 | ||||
chr15:52179923-52180070 | Rare:51 | ||||
chr15:55319049-55319248 | Common:3; Rare:53 |