| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4616249-4616524 | Rare:71 | ||||
| chr16:4693453-4693747 | Common:3; Rare:130 | ||||
| chr16:4734179-4734534 | Common:1; Rare:117 | ||||
| chr16:4767148-4767296 | Common:1; Rare:48 | ||||
| chr16:4847248-4847481 | Common:2; Rare:106 | ||||
| chr16:4891809-4892234 | Common:5; Rare:206 | ||||
| chr16:4893211-4893642 | Common:1; Rare:169 | ||||
| chr16:4936978-4937419 | Common:6; Rare:161 | ||||
| chr16:5033926-5033941 | Rare:3 | ||||
| chr16:5097728-5097932 | Common:4; Rare:80 | ||||
| chr16:8621625-8621745 | Common:1; Rare:44 | ||||
| chr16:8797612-8797891 | Common:1; Rare:112; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868966-8869291 | Common:5; Rare:144 | ||||
| chr16:9092101-9092197 | Rare:32 | ||||
| chr16:10580557-10580740 | Rare:57 |