| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1420719-1420975 | Common:1; Rare:105 | ||||
| chr16:1493263-1493587 | Common:4; Rare:98 | ||||
| chr16:1533487-1533683 | Common:1; Rare:40 | ||||
| chr16:1706047-1706286 | Common:2; Rare:70 | ||||
| chr16:1771525-1771604 | Rare:32 | ||||
| chr16:1782821-1783009 | Rare:62 | ||||
| chr16:1959407-1959634 | Common:5; Rare:102 | ||||
| chr16:1971932-1972110 | Common:1; Rare:50 | ||||
| chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155451-2155820 | Common:1; Rare:104 | ||||
| chr16:2268060-2268178 | Common:1; Rare:62 | ||||
| chr16:2459980-2460112 | Rare:33 | ||||
| chr16:2513659-2514011 | Rare:121 | ||||
| chr16:2682359-2682598 | Rare:109 | ||||
| chr16:2777072-2777366 | Common:2; Rare:109 |