| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:684326-684464 | Common:2; Rare:72 | ||||
| chr16:720483-720595 | Common:1; Rare:28 | ||||
| chr16:740891-741152 | Common:1; Rare:91 | ||||
| chr16:970826-971195 | Common:7; Rare:167 | ||||
| chr16:980784-981112 | Common:4; Rare:87 | ||||
| chr16:1420707-1420975 | Common:1; Rare:112 | ||||
| chr16:1493251-1493591 | Common:4; Rare:104 | ||||
| chr16:1612011-1612357 | Common:1; Rare:115; Clinvar:2 | ||||
| chr16:1706042-1706330 | Common:2; Rare:92 | ||||
| chr16:1771502-1771868 | Common:3; Rare:144 | ||||
| chr16:1773071-1773209 | Rare:44; Clinvar (pathogenic):1 | ||||
| chr16:1782508-1783012 | Common:4; Rare:166 | ||||
| chr16:1826785-1826975 | Common:3; Rare:62 | ||||
| chr16:1827144-1827509 | Common:3; Rare:184 | ||||
| chr16:1943142-1943539 | Common:1; Rare:128 |