| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1420708-1420907 | Common:1; Rare:84 | ||||
| chr16:1493258-1493587 | Common:4; Rare:100 | ||||
| chr16:1706069-1706387 | Common:3; Rare:98 | ||||
| chr16:1773128-1773177 | Rare:9 | ||||
| chr16:1782509-1783023 | Common:4; Rare:172 | ||||
| chr16:1826790-1826912 | Common:1; Rare:42 | ||||
| chr16:1827179-1827340 | Rare:88 | ||||
| chr16:1943207-1943503 | Common:1; Rare:86 | ||||
| chr16:1959458-1959634 | Common:3; Rare:83 | ||||
| chr16:1964557-1964978 | Common:15; Rare:192 | ||||
| chr16:1971927-1972106 | Common:1; Rare:49 | ||||
| chr16:2009694-2009896 | Common:14; Rare:82 | ||||
| chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2205729-2205889 | Common:3; Rare:72 | ||||
| chr16:2268069-2268520 | Common:5; Rare:156 |