| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4957734-4957949 | Common:2; Rare:64 | ||||
| chr16:5033368-5033398 | Rare:7 | ||||
| chr16:5033535-5033724 | Common:1; Rare:93; Clinvar:1 | ||||
| chr16:5033834-5034023 | Rare:80 | ||||
| chr16:5071753-5071954 | Rare:111; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:5072090-5072152 | Rare:20 | ||||
| chr16:5097682-5098199 | Common:4; Rare:172 | ||||
| chr16:8621558-8621786 | Common:1; Rare:91 | ||||
| chr16:8674368-8674698 | Common:2; Rare:111; Clinvar:2 | ||||
| chr16:8797544-8797923 | Common:3; Rare:157; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:8798184-8798336 | Common:3; Rare:35 | ||||
| chr16:8868344-8868553 | Rare:52 | ||||
| chr16:8868643-8868804 | Rare:45 | ||||
| chr16:8868954-8869315 | Common:6; Rare:162 | ||||
| chr16:8962273-8962503 | Common:2; Rare:65 |