| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1612037-1612391 | Common:2; Rare:127; Clinvar:1 | ||||
| chr16:1706056-1706411 | Common:4; Rare:110 | ||||
| chr16:1771499-1771811 | Common:2; Rare:113 | ||||
| chr16:1773110-1773207 | Rare:29 | ||||
| chr16:1782510-1783023 | Common:4; Rare:171 | ||||
| chr16:1959416-1959656 | Common:5; Rare:105 | ||||
| chr16:1964819-1965061 | Common:6; Rare:105 | ||||
| chr16:1971913-1972113 | Common:1; Rare:59 | ||||
| chr16:2047795-2048053 | Rare:124; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:2205736-2205860 | Common:3; Rare:54 | ||||
| chr16:2268066-2268227 | Common:1; Rare:69 | ||||
| chr16:2268393-2268471 | Rare:27 | ||||
| chr16:2459976-2460109 | Rare:33 | ||||
| chr16:2475000-2475156 | Rare:53; Clinvar (benign):2 | ||||
| chr16:2513645-2514005 | Rare:122 |