| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15856922-15857223 | Common:4; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:15857270-15857385 | Common:2; Rare:29 | ||||
| chr16:18790249-18790449 | Common:4; Rare:75 | ||||
| chr16:18926115-18926213 | Common:2; Rare:45 | ||||
| chr16:19067552-19067723 | Common:4; Rare:94; Clinvar:1 | ||||
| chr16:19067773-19067941 | Common:2; Rare:41 | ||||
| chr16:19521746-19521781 | Rare:14 | ||||
| chr16:19555407-19555733 | Common:2; Rare:142 | ||||
| chr16:20676160-20676185 | Rare:5 | ||||
| chr16:20741518-20741587 | Rare:18 | ||||
| chr16:20763942-20764063 | Common:1; Rare:21 | ||||
| chr16:20806338-20806617 | Rare:93 | ||||
| chr16:20900226-20900873 | Common:4; Rare:154 | ||||
| chr16:21652602-21652733 | Rare:31 | ||||
| chr16:21953021-21953413 | Common:1; Rare:99; Clinvar (benign):3 |