| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1773320-1773650 | Common:3; Rare:236 | ||||
| chr16:1782485-1783043 | Common:7; Rare:306 | ||||
| chr16:1826785-1826977 | Common:3; Rare:62 | ||||
| chr16:1827144-1827510 | Common:4; Rare:248 | ||||
| chr16:1943163-1943513 | Common:1; Rare:110 | ||||
| chr16:1959373-1959680 | Common:11; Rare:231 | ||||
| chr16:1964588-1965130 | Common:37; Rare:415 | ||||
| chr16:1971879-1972145 | Common:6; Rare:156 | ||||
| chr16:1983890-1984348 | Common:12; Rare:239; Clinvar (benign):7 | ||||
| chr16:2009661-2009983 | Common:31; Rare:262 | ||||
| chr16:2047727-2048087 | Rare:294; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr16:2135883-2136188 | Common:1; Rare:144 | ||||
| chr16:2148266-2148900 | Common:1; Rare:244 | ||||
| chr16:2155289-2155837 | Common:4; Rare:359 | ||||
| chr16:2163340-2164006 | Common:5; Rare:271 |