| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5071775-5071861 | Rare:40; Clinvar (benign):1 | ||||
| chr16:8797618-8797889 | Rare:106; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868973-8869274 | Common:4; Rare:133 | ||||
| chr16:10580585-10580867 | Common:2; Rare:95 | ||||
| chr16:10944327-10944591 | Common:1; Rare:77 | ||||
| chr16:11586887-11587005 | Common:1; Rare:36 | ||||
| chr16:11797173-11797499 | Common:2; Rare:124 | ||||
| chr16:11851513-11851635 | Rare:60 | ||||
| chr16:11915876-11916208 | Common:2; Rare:135 | ||||
| chr16:11976604-11976760 | Common:3; Rare:62 | ||||
| chr16:14630178-14630404 | Rare:96 | ||||
| chr16:14632729-14632989 | Common:1; Rare:85 | ||||
| chr16:15094247-15094367 | Rare:58 | ||||
| chr16:15888581-15888874 | Common:5; Rare:98 | ||||
| chr16:18790237-18790461 | Common:4; Rare:82 |