| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8622090-8622284 | Common:6; Rare:47 | ||||
| chr16:8674434-8674714 | Common:1; Rare:92; Clinvar:3 | ||||
| chr16:8797387-8797506 | Common:3; Rare:34 | ||||
| chr16:8797513-8797939 | Common:3; Rare:176; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr16:8868326-8868549 | Rare:52 | ||||
| chr16:8868604-8868776 | Rare:46 | ||||
| chr16:8868943-8869173 | Common:3; Rare:112 | ||||
| chr16:8962501-8962919 | Common:4; Rare:143 | ||||
| chr16:8963398-8963534 | Common:1; Rare:26 | ||||
| chr16:8963796-8964135 | Common:3; Rare:124 | ||||
| chr16:9091085-9091773 | Common:3; Rare:284 | ||||
| chr16:9091850-9092138 | Rare:108 | ||||
| chr16:9092251-9092377 | Rare:51 | ||||
| chr16:9092428-9092626 | Common:2; Rare:72 | ||||
| chr16:9092685-9092722 | Common:1; Rare:10 |