| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30949187-30949341 | Common:2; Rare:52 | ||||
| chr16:30997284-30997403 | Common:1; Rare:28 | ||||
| chr16:31033294-31033601 | Common:2; Rare:99 | ||||
| chr16:31074187-31074456 | Common:1; Rare:75 | ||||
| chr16:31108285-31108465 | Rare:41 | ||||
| chr16:31202295-31202553 | Common:2; Rare:79 | ||||
| chr16:31442787-31443061 | Common:1; Rare:42 | ||||
| chr16:31471896-31472200 | Rare:69 | ||||
| chr16:31508374-31508484 | Common:2; Rare:43 | ||||
| chr16:46621316-46621483 | Rare:64 | ||||
| chr16:46689134-46689277 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689465-46689708 | Common:2; Rare:90; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46831115-46831576 | Common:3; Rare:155 | ||||
| chr16:46973577-46973797 | Rare:98 | ||||
| chr16:47461032-47461378 | Common:2; Rare:135; Clinvar (benign):2 |