| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1611969-1612362 | Common:2; Rare:135; Clinvar:2 | ||||
| chr16:1678002-1678336 | Common:3; Rare:112 | ||||
| chr16:1706033-1706370 | Common:3; Rare:111 | ||||
| chr16:1771515-1771889 | Common:4; Rare:145 | ||||
| chr16:1773126-1773207 | Rare:19 | ||||
| chr16:1782508-1783023 | Common:4; Rare:172 | ||||
| chr16:1826716-1826975 | Common:3; Rare:86 | ||||
| chr16:1827171-1827259 | Common:1; Rare:51 | ||||
| chr16:1943160-1943527 | Common:1; Rare:116 | ||||
| chr16:1959394-1959656 | Common:5; Rare:111 | ||||
| chr16:1964809-1964992 | Common:6; Rare:83 | ||||
| chr16:1971883-1972129 | Common:3; Rare:73 | ||||
| chr16:2009674-2009998 | Common:17; Rare:140 | ||||
| chr16:2047770-2048050 | Rare:136; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155641-2155825 | Common:2; Rare:53 |