| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:12901456-12901635 | Common:1; Rare:31 | ||||
| chr16:14071060-14071365 | Common:2; Rare:106 | ||||
| chr16:14186475-14186690 | Rare:36 | ||||
| chr16:14630195-14630433 | Rare:103 | ||||
| chr16:14632743-14632995 | Common:1; Rare:83 | ||||
| chr16:15094237-15094442 | Common:1; Rare:98 | ||||
| chr16:15395908-15396021 | Rare:40 | ||||
| chr16:15650036-15650285 | Common:1; Rare:124 | ||||
| chr16:15857010-15857151 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr16:18790256-18790434 | Common:4; Rare:68 | ||||
| chr16:18801456-18801830 | Common:4; Rare:132 | ||||
| chr16:18926397-18926605 | Common:2; Rare:92 | ||||
| chr16:19067422-19067715 | Common:5; Rare:121; Clinvar:1 | ||||
| chr16:19067817-19068025 | Common:1; Rare:52 | ||||
| chr16:19521995-19522239 | Rare:64 |