Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:50693515-50693619 | Rare:42 | ||||
chr16:50742685-50742782 | Rare:19 | ||||
chr16:53435506-53435642 | Common:1; Rare:26 | ||||
chr16:53703809-53704213 | Common:1; Rare:129; Clinvar:4; Clinvar (benign):2 | ||||
chr16:54286785-54287007 | Common:1; Rare:67 | ||||
chr16:55479037-55479217 | Rare:43 | ||||
chr16:55479412-55479626 | Common:1; Rare:78; Clinvar:4; Clinvar (benign):1 | ||||
chr16:56451274-56451626 | Common:1; Rare:113 | ||||
chr16:56608407-56608752 | Common:3; Rare:103 | ||||
chr16:56608839-56609058 | Rare:57 | ||||
chr16:56625403-56625630 | Common:1; Rare:48 | ||||
chr16:56625642-56625845 | Rare:61 | ||||
chr16:56632185-56632724 | Common:2; Rare:162 | ||||
chr16:56682058-56682571 | Common:9; Rare:147 | ||||
chr16:56729945-56730208 | Common:1; Rare:64 |