| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70476547-70477064 | Common:2; Rare:96 | ||||
| chr16:70522678-70522702 | Rare:4 | ||||
| chr16:70523186-70523311 | Common:2; Rare:25 | ||||
| chr16:70523468-70523884 | Common:3; Rare:152; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70523978-70524048 | Rare:17 | ||||
| chr16:70524221-70524550 | Common:2; Rare:84 | ||||
| chr16:70800889-70800903 | Rare:4 | ||||
| chr16:70801032-70801291 | Common:2; Rare:90 | ||||
| chr16:71288727-71288940 | Rare:49 | ||||
| chr16:71289128-71289530 | Common:2; Rare:104 | ||||
| chr16:71289720-71289771 | Rare:12 | ||||
| chr16:71462128-71462373 | Common:3; Rare:92 | ||||
| chr16:71484153-71484334 | Common:2; Rare:45 | ||||
| chr16:71484529-71484744 | Common:1; Rare:48 | ||||
| chr16:71526361-71526441 | Rare:17 |