| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5033336-5033398 | Rare:20 | ||||
| chr16:5033479-5033747 | Common:2; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:5033832-5034015 | Rare:80 | ||||
| chr16:5071760-5071961 | Rare:110; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:5072110-5072159 | Rare:14 | ||||
| chr16:5097681-5098150 | Common:4; Rare:156 | ||||
| chr16:8572745-8572850 | Common:1; Rare:29 | ||||
| chr16:8621555-8621796 | Common:1; Rare:93 | ||||
| chr16:8622085-8622349 | Common:6; Rare:62 | ||||
| chr16:8674384-8674712 | Common:1; Rare:113; Clinvar:3 | ||||
| chr16:8797365-8797457 | Common:2; Rare:29 | ||||
| chr16:8797559-8797943 | Common:3; Rare:163; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr16:8868324-8868479 | Rare:35 | ||||
| chr16:8868616-8868868 | Rare:68 | ||||
| chr16:8868921-8869312 | Common:6; Rare:175 |