| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15719275-15719538 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:15719639-15719847 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):2 | ||||
| chr16:15735593-15735746 | Common:3; Rare:34 | ||||
| chr16:15759663-15759963 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:17483588-17483875 | Common:3; Rare:45 | ||||
| chr16:19120559-19120892 | Common:6; Rare:73 | ||||
| chr16:19393732-19393973 | Common:1; Rare:62 | ||||
| chr16:21501568-21501754 | Rare:25 | ||||
| chr16:21501965-21502119 | Common:1; Rare:33 | ||||
| chr16:21820410-21820603 | Rare:61 | ||||
| chr16:23755233-23755466 | Common:1; Rare:51 | ||||
| chr16:23755642-23756204 | Common:1; Rare:175 | ||||
| chr16:24844675-24844807 | Common:1; Rare:23 | ||||
| chr16:24918983-24919113 | Common:1; Rare:28 | ||||
| chr16:27286026-27286234 | Rare:25 |