| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:636223-636458 | Common:4; Rare:73 | ||||
| chr16:649252-649395 | Common:1; Rare:51 | ||||
| chr16:680318-680520 | Common:2; Rare:68 | ||||
| chr16:684326-684457 | Common:2; Rare:70 | ||||
| chr16:690346-690482 | Common:3; Rare:62 | ||||
| chr16:740938-741141 | Rare:68 | ||||
| chr16:1351821-1351980 | Common:2; Rare:81; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1420695-1420937 | Common:1; Rare:104 | ||||
| chr16:1421109-1421221 | Common:5; Rare:31 | ||||
| chr16:1533484-1533694 | Common:1; Rare:40 | ||||
| chr16:1612032-1612335 | Common:1; Rare:98; Clinvar:1 | ||||
| chr16:1706047-1706321 | Common:2; Rare:85 | ||||
| chr16:1772677-1773034 | Common:4; Rare:118; Clinvar (pathogenic):2 | ||||
| chr16:1773110-1773207 | Rare:29 | ||||
| chr16:1782508-1783019 | Common:4; Rare:170 |