| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1612037-1612354 | Common:1; Rare:104; Clinvar:1 | ||||
| chr16:1763858-1763957 | Rare:19 | ||||
| chr16:1771499-1771602 | Rare:44 | ||||
| chr16:1772834-1772871 | Rare:8 | ||||
| chr16:1782510-1782815 | Common:4; Rare:102 | ||||
| chr16:1782821-1783015 | Rare:64 | ||||
| chr16:1826790-1826975 | Common:3; Rare:61 | ||||
| chr16:1827179-1827240 | Rare:34 | ||||
| chr16:1943165-1943535 | Common:1; Rare:116 | ||||
| chr16:1959416-1959653 | Common:5; Rare:103 | ||||
| chr16:1964802-1965066 | Common:6; Rare:122 | ||||
| chr16:1971801-1972142 | Common:3; Rare:103 | ||||
| chr16:1992207-1992541 | Common:4; Rare:85 | ||||
| chr16:2047770-2048050 | Rare:136; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155464-2155833 | Common:2; Rare:104 |