| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1379560-1379796 | Common:2; Rare:99 | ||||
| chr16:1414692-1414919 | Common:5; Rare:61 | ||||
| chr16:1420679-1420949 | Common:2; Rare:120 | ||||
| chr16:1493258-1493587 | Common:4; Rare:100 | ||||
| chr16:1612032-1612335 | Common:1; Rare:98; Clinvar:1 | ||||
| chr16:1706042-1706300 | Common:2; Rare:83 | ||||
| chr16:1771494-1771868 | Common:3; Rare:149 | ||||
| chr16:1772602-1772892 | Common:3; Rare:98; Clinvar (pathogenic):2 | ||||
| chr16:1773076-1773209 | Rare:43; Clinvar (pathogenic):1 | ||||
| chr16:1782508-1783019 | Common:4; Rare:170 | ||||
| chr16:1826789-1826994 | Common:4; Rare:67 | ||||
| chr16:1827171-1827241 | Common:1; Rare:37 | ||||
| chr16:1943133-1943529 | Common:1; Rare:127 | ||||
| chr16:1959391-1959734 | Common:6; Rare:147 | ||||
| chr16:1964761-1965074 | Common:15; Rare:141 |