| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1772654-1772814 | Common:2; Rare:57; Clinvar (pathogenic):2 | ||||
| chr16:1773117-1773207 | Rare:23 | ||||
| chr16:1782508-1782721 | Common:3; Rare:68 | ||||
| chr16:1782788-1783009 | Rare:75 | ||||
| chr16:1826790-1826994 | Common:4; Rare:67 | ||||
| chr16:1827179-1827502 | Common:2; Rare:171 | ||||
| chr16:1943183-1943506 | Common:1; Rare:99 | ||||
| chr16:1964822-1965076 | Common:7; Rare:104 | ||||
| chr16:1971997-1972079 | Common:1; Rare:29 | ||||
| chr16:2047824-2048038 | Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2268071-2268459 | Common:4; Rare:134 | ||||
| chr16:2513650-2514005 | Rare:120 | ||||
| chr16:2777238-2777392 | Common:1; Rare:64 | ||||
| chr16:2858168-2858230 | Rare:14 | ||||
| chr16:3020225-3020381 | Rare:59 |