| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19884824-19884987 | Common:2; Rare:57 | ||||
| chr16:20741326-20741542 | Common:5; Rare:67 | ||||
| chr16:20741662-20742012 | Common:1; Rare:148 | ||||
| chr16:20806326-20806739 | Rare:122 | ||||
| chr16:20806857-20806999 | Rare:31 | ||||
| chr16:20807130-20807236 | Rare:28 | ||||
| chr16:20900085-20900992 | Common:6; Rare:207 | ||||
| chr16:20901462-20901629 | Common:1; Rare:29 | ||||
| chr16:21158515-21158722 | Common:1; Rare:60 | ||||
| chr16:21599292-21599671 | Common:4; Rare:128 | ||||
| chr16:21599726-21600191 | Common:1; Rare:151 | ||||
| chr16:21611630-21611788 | Common:1; Rare:34 | ||||
| chr16:21611987-21612092 | Rare:14 | ||||
| chr16:21612259-21612325 | Rare:13 | ||||
| chr16:21952970-21953454 | Common:1; Rare:124; Clinvar (benign):3 |