| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1612620-1613109 | Common:6; Rare:273 | ||||
| chr16:1613997-1614397 | Common:3; Rare:136 | ||||
| chr16:1614450-1614800 | Rare:88 | ||||
| chr16:1614801-1615201 | Common:4; Rare:145 | ||||
| chr16:1677904-1678343 | Common:15; Rare:565 | ||||
| chr16:1678312-1678682 | Common:4; Rare:122 | ||||
| chr16:1679877-1680277 | Rare:138 | ||||
| chr16:1705467-1705867 | Common:4; Rare:82 | ||||
| chr16:1705925-1706403 | Common:18; Rare:649 | ||||
| chr16:1706634-1707252 | Common:4; Rare:149 | ||||
| chr16:1763154-1764070 | Common:6; Rare:450 | ||||
| chr16:1771385-1772020 | Common:22; Rare:1075 | ||||
| chr16:1772059-1772739 | Common:7; Rare:765; Clinvar (pathogenic):1 | ||||
| chr16:1772643-1772915 | Common:8; Rare:297; Clinvar (pathogenic):5 | ||||
| chr16:1772971-1773379 | Common:4; Rare:570; Clinvar (pathogenic):7 |