| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31713115-31713411 | Common:1; Rare:73 | ||||
| chr16:31713545-31713660 | Common:1; Rare:32 | ||||
| chr16:31873596-31873900 | Common:1; Rare:97 | ||||
| chr16:31874100-31874179 | Rare:8 | ||||
| chr16:31874369-31874471 | Rare:12 | ||||
| chr16:46621293-46621533 | Common:1; Rare:89 | ||||
| chr16:46688622-46688789 | Rare:41 | ||||
| chr16:46689107-46689272 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689487-46689760 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46689851-46689930 | Rare:24 | ||||
| chr16:46690105-46690261 | Rare:37 | ||||
| chr16:46789688-46790159 | Common:5; Rare:102 | ||||
| chr16:46830779-46830821 | Rare:12 | ||||
| chr16:46831042-46831335 | Common:2; Rare:105 | ||||
| chr16:46883998-46884446 | Common:3; Rare:121 |