| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1420679-1421007 | Common:2; Rare:140 | ||||
| chr16:1458802-1459046 | Common:4; Rare:57 | ||||
| chr16:1459140-1459283 | Common:1; Rare:42; Clinvar:1 | ||||
| chr16:1493233-1493592 | Common:4; Rare:109 | ||||
| chr16:1706079-1706241 | Common:1; Rare:50 | ||||
| chr16:1767713-1767891 | Common:3; Rare:59 | ||||
| chr16:1773120-1773214 | Rare:25 | ||||
| chr16:1782506-1783009 | Common:4; Rare:167 | ||||
| chr16:1827157-1827227 | Common:1; Rare:30 | ||||
| chr16:1943142-1943489 | Common:1; Rare:110 | ||||
| chr16:1964819-1965066 | Common:6; Rare:105 | ||||
| chr16:1971900-1972110 | Common:1; Rare:60 | ||||
| chr16:2047769-2048045 | Rare:131; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2268056-2268184 | Common:1; Rare:67 | ||||
| chr16:2474988-2475149 | Rare:51 |