| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67968577-67968812 | Common:2; Rare:85 | ||||
| chr16:68023209-68023302 | Common:1; Rare:25 | ||||
| chr16:68310922-68311062 | Common:1; Rare:67 | ||||
| chr16:69132528-69132663 | Rare:51 | ||||
| chr16:69726446-69726727 | Common:3; Rare:73 | ||||
| chr16:70346760-70346929 | Common:1; Rare:77 | ||||
| chr16:70523527-70523844 | Common:3; Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:71289360-71289653 | Common:2; Rare:95 | ||||
| chr16:71895348-71895540 | Rare:55 | ||||
| chr16:72093602-72093944 | Rare:80 | ||||
| chr16:74701133-74701344 | Common:1; Rare:47 | ||||
| chr16:75647635-75647786 | Common:1; Rare:72; Clinvar:3 | ||||
| chr16:81006839-81007223 | Common:3; Rare:124 | ||||
| chr16:84116902-84117042 | Common:1; Rare:52 | ||||
| chr16:85799535-85799745 | Common:2; Rare:62 |