| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4681173-4681377 | Common:1; Rare:51 | ||||
| chr16:4693410-4693785 | Common:3; Rare:168 | ||||
| chr16:4693789-4693889 | Common:1; Rare:31 | ||||
| chr16:4694124-4694240 | Rare:51 | ||||
| chr16:4733847-4733910 | Rare:14 | ||||
| chr16:4734090-4734635 | Common:3; Rare:202 | ||||
| chr16:4734814-4735012 | Common:1; Rare:66 | ||||
| chr16:4767103-4767601 | Common:4; Rare:147 | ||||
| chr16:4795139-4795408 | Rare:83 | ||||
| chr16:4800431-4800513 | Rare:38; Clinvar (pathogenic):1 | ||||
| chr16:4802126-4802419 | Common:1; Rare:157; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:4802595-4802832 | Rare:79; Clinvar:5 | ||||
| chr16:4846490-4846718 | Common:2; Rare:68 | ||||
| chr16:4847058-4847106 | Common:2; Rare:21 | ||||
| chr16:4847194-4847566 | Common:4; Rare:175 |