| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30698425-30698822 | Common:2; Rare:141 | ||||
| chr16:30698868-30699177 | Common:1; Rare:116; Clinvar (benign):1 | ||||
| chr16:30699242-30699452 | Rare:39 | ||||
| chr16:30748039-30748469 | Common:2; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30748778-30748827 | Rare:15 | ||||
| chr16:30761433-30761614 | Rare:70 | ||||
| chr16:30762045-30762390 | Common:3; Rare:112 | ||||
| chr16:30762537-30762566 | Rare:5 | ||||
| chr16:30762962-30763003 | Rare:12 | ||||
| chr16:30787165-30787375 | Common:1; Rare:39 | ||||
| chr16:30787493-30787574 | Rare:7 | ||||
| chr16:30787595-30787612 | Rare:3 | ||||
| chr16:30893990-30894421 | Common:5; Rare:109 | ||||
| chr16:30896975-30897378 | Common:1; Rare:64 | ||||
| chr16:30922470-30923113 | Common:2; Rare:186 |