| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:50742727-50742782 | Rare:10 | ||||
| chr16:53054858-53055055 | Common:1; Rare:46 | ||||
| chr16:53434651-53434692 | Rare:19 | ||||
| chr16:53435492-53435679 | Common:1; Rare:38 | ||||
| chr16:53703815-53704206 | Common:1; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286623-54287028 | Common:2; Rare:113 | ||||
| chr16:54930568-54930734 | Common:1; Rare:43 | ||||
| chr16:55509023-55509276 | Common:2; Rare:79 | ||||
| chr16:55557317-55557546 | Rare:37 | ||||
| chr16:56451260-56451615 | Common:1; Rare:115 | ||||
| chr16:56608379-56608752 | Common:3; Rare:113 | ||||
| chr16:56625647-56625865 | Rare:66 | ||||
| chr16:56632200-56632668 | Common:2; Rare:133 | ||||
| chr16:56638533-56638669 | Rare:57 | ||||
| chr16:56729975-56730202 | Common:1; Rare:52 |