Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4847231-4847436 | Common:1; Rare:89 | ||||
chr16:5033920-5033955 | Rare:14 | ||||
chr16:5097728-5098026 | Common:4; Rare:104 | ||||
chr16:8797631-8797877 | Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr16:10580573-10580756 | Rare:58 | ||||
chr16:10878767-10878995 | Rare:51 | ||||
chr16:10944332-10944645 | Common:1; Rare:98 | ||||
chr16:11851511-11851635 | Rare:61 | ||||
chr16:11915882-11916235 | Common:2; Rare:142 | ||||
chr16:11976615-11976766 | Common:2; Rare:57 | ||||
chr16:14186475-14186911 | Rare:79 | ||||
chr16:14974651-14975191 | Common:2; Rare:143 | ||||
chr16:14997506-14997780 | Common:1; Rare:49 | ||||
chr16:15094247-15094392 | Rare:73 | ||||
chr16:15601609-15601902 | Common:4; Rare:64 |