| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31117892-31118059 | Rare:41 | ||||
| chr16:31129860-31130104 | Rare:66 | ||||
| chr16:31135647-31135842 | Rare:47 | ||||
| chr16:31179827-31180205 | Common:3; Rare:165; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31202658-31202772 | Rare:50 | ||||
| chr16:31442763-31443059 | Common:1; Rare:48 | ||||
| chr16:31458199-31458311 | Common:1; Rare:32 | ||||
| chr16:31458897-31459161 | Rare:76 | ||||
| chr16:31459288-31459522 | Common:1; Rare:98 | ||||
| chr16:31472119-31472198 | Rare:23 | ||||
| chr16:31487715-31488048 | Common:1; Rare:96; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:31508365-31508484 | Common:2; Rare:49 | ||||
| chr16:46689129-46689317 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973532-46973789 | Rare:103 | ||||
| chr16:47460938-47461383 | Common:2; Rare:184; Clinvar (benign):2 |