Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1773117-1773191 | Rare:16 | ||||
chr16:1782508-1782827 | Common:4; Rare:104 | ||||
chr16:1964814-1964982 | Common:6; Rare:75 | ||||
chr16:1971791-1972077 | Common:3; Rare:85 | ||||
chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268055-2268209 | Common:1; Rare:72 | ||||
chr16:2268393-2268497 | Rare:39 | ||||
chr16:2475003-2475131 | Rare:42 | ||||
chr16:2682350-2682628 | Rare:131 | ||||
chr16:2720187-2720238 | Rare:14 | ||||
chr16:2777023-2777350 | Common:2; Rare:112 | ||||
chr16:2856692-2856856 | Common:1; Rare:46 | ||||
chr16:2857607-2857628 | |||||
chr16:2858149-2858172 | Rare:5 | ||||
chr16:2911746-2912018 | Common:3; Rare:92 |