| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1533487-1533718 | Common:1; Rare:47 | ||||
| chr16:1612032-1612354 | Common:1; Rare:105; Clinvar:1 | ||||
| chr16:1706056-1706387 | Common:3; Rare:104 | ||||
| chr16:1771488-1771853 | Common:3; Rare:147 | ||||
| chr16:1773115-1773191 | Rare:18 | ||||
| chr16:1782653-1783010 | Common:1; Rare:112 | ||||
| chr16:1826783-1826975 | Common:3; Rare:64 | ||||
| chr16:1827147-1827247 | Common:1; Rare:48 | ||||
| chr16:1943189-1943503 | Common:1; Rare:94 | ||||
| chr16:1964493-1964944 | Common:15; Rare:188 | ||||
| chr16:1971906-1972113 | Common:1; Rare:61 | ||||
| chr16:2009694-2009896 | Common:14; Rare:82 | ||||
| chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2223304-2223636 | Rare:132 | ||||
| chr16:2268063-2268210 | Common:1; Rare:64 |