| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:680327-680472 | Common:2; Rare:48 | ||||
| chr16:970856-971139 | Common:7; Rare:133 | ||||
| chr16:1309354-1309723 | Rare:137 | ||||
| chr16:1351868-1351974 | Common:1; Rare:49; Clinvar:5; Clinvar (benign):1 | ||||
| chr16:1414692-1414919 | Common:5; Rare:61 | ||||
| chr16:1420705-1420985 | Common:1; Rare:117 | ||||
| chr16:1533487-1533694 | Common:1; Rare:40 | ||||
| chr16:1612037-1612335 | Common:1; Rare:97; Clinvar:1 | ||||
| chr16:1782510-1782878 | Common:4; Rare:119 | ||||
| chr16:1943189-1943513 | Common:1; Rare:99 | ||||
| chr16:1964824-1964979 | Common:6; Rare:63 | ||||
| chr16:1971885-1972113 | Common:3; Rare:66 | ||||
| chr16:2047795-2048050 | Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2205697-2205875 | Common:4; Rare:84 | ||||
| chr16:2223304-2223659 | Rare:142 |