Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:8797631-8797877 | Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr16:10580581-10580843 | Common:2; Rare:90 | ||||
chr16:10944333-10944592 | Common:1; Rare:76 | ||||
chr16:11851406-11851647 | Common:1; Rare:123 | ||||
chr16:11915883-11916208 | Common:2; Rare:134 | ||||
chr16:11976628-11976775 | Rare:58 | ||||
chr16:14071048-14071355 | Common:3; Rare:106 | ||||
chr16:14186576-14186734 | Rare:31 | ||||
chr16:14630195-14630484 | Rare:113 | ||||
chr16:14632754-14632999 | Common:1; Rare:79 | ||||
chr16:14997696-14997820 | Common:1; Rare:41 | ||||
chr16:15094238-15094409 | Common:1; Rare:84 | ||||
chr16:15395912-15396008 | Rare:35 | ||||
chr16:15643037-15643267 | Rare:72 | ||||
chr16:15650057-15650283 | Common:1; Rare:113 |