| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19486696-19486992 | Common:2; Rare:66 | ||||
| chr16:19521942-19522152 | Rare:65 | ||||
| chr16:19555455-19555729 | Common:1; Rare:123 | ||||
| chr16:19884772-19884963 | Common:2; Rare:65 | ||||
| chr16:20741551-20741591 | Rare:12 | ||||
| chr16:20763903-20764069 | Common:2; Rare:26 | ||||
| chr16:20806331-20806705 | Rare:114 | ||||
| chr16:20900210-20900899 | Common:4; Rare:161 | ||||
| chr16:21158542-21158735 | Common:1; Rare:56 | ||||
| chr16:21233592-21233731 | Rare:31 | ||||
| chr16:21599383-21599807 | Common:4; Rare:152 | ||||
| chr16:21652600-21652949 | Rare:67 | ||||
| chr16:21952975-21953517 | Common:1; Rare:135; Clinvar (benign):3 | ||||
| chr16:22206518-22206652 | Rare:33 | ||||
| chr16:22436912-22437359 | Rare:151 |