| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69131615-69131837 | Common:1; Rare:47 | ||||
| chr16:69132100-69132708 | Common:1; Rare:149 | ||||
| chr16:69133377-69133394 | Rare:4 | ||||
| chr16:69186984-69187290 | Rare:99 | ||||
| chr16:69187352-69187472 | Rare:23 | ||||
| chr16:69187676-69187815 | Rare:33 | ||||
| chr16:69187832-69188089 | Common:1; Rare:61 | ||||
| chr16:69311013-69311490 | Common:1; Rare:132 | ||||
| chr16:69329109-69329278 | Rare:79; Clinvar (benign):1 | ||||
| chr16:69329870-69330162 | Common:4; Rare:131 | ||||
| chr16:69330184-69330375 | Common:1; Rare:67 | ||||
| chr16:69330482-69330849 | Common:3; Rare:170; Clinvar (benign):2 | ||||
| chr16:69339229-69339349 | Rare:39; Clinvar:1 | ||||
| chr16:69339480-69339932 | Common:2; Rare:194; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:69340024-69340083 | Rare:25 |