| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1351837-1351971 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:1533487-1533768 | Common:1; Rare:57 | ||||
| chr16:1773110-1773209 | Rare:29 | ||||
| chr16:1782510-1783012 | Common:4; Rare:165 | ||||
| chr16:1826602-1826938 | Common:3; Rare:101 | ||||
| chr16:1827126-1827229 | Common:1; Rare:42 | ||||
| chr16:1943123-1943497 | Common:1; Rare:118 | ||||
| chr16:1964814-1965011 | Common:6; Rare:89 | ||||
| chr16:1971937-1972123 | Common:1; Rare:54 | ||||
| chr16:2047727-2048033 | Rare:146; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2268072-2268171 | Rare:45 | ||||
| chr16:2475025-2475155 | Rare:48; Clinvar (benign):2 | ||||
| chr16:2777242-2777389 | Common:1; Rare:61 | ||||
| chr16:3134849-3135166 | Common:3; Rare:86 | ||||
| chr16:3305268-3305514 | Common:3; Rare:77 |