| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31459281-31459522 | Common:1; Rare:101 | ||||
| chr16:31487719-31488048 | Common:1; Rare:94; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:31508365-31508484 | Common:2; Rare:49 | ||||
| chr16:46689134-46689313 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973577-46973789 | Rare:93 | ||||
| chr16:47460938-47461365 | Common:2; Rare:171; Clinvar (benign):2 | ||||
| chr16:48244254-48244492 | Common:2; Rare:72 | ||||
| chr16:48244498-48244575 | Rare:21 | ||||
| chr16:53054907-53055055 | Common:1; Rare:29 | ||||
| chr16:53703821-53704221 | Common:1; Rare:126; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:56451312-56451567 | Common:1; Rare:70 | ||||
| chr16:56625670-56625876 | Rare:66 | ||||
| chr16:56632461-56632749 | Common:2; Rare:93 | ||||
| chr16:56657456-56657826 | Common:1; Rare:79 | ||||
| chr16:56668486-56668596 | Common:1; Rare:20 |