| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4788272-4788452 | Common:1; Rare:51 | ||||
| chr16:4802878-4803082 | Common:2; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:4847226-4847672 | Common:3; Rare:199 | ||||
| chr16:4848017-4848124 | Common:1; Rare:33 | ||||
| chr16:5033920-5033997 | Rare:30 | ||||
| chr16:5071778-5071910 | Rare:79; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:5097697-5097988 | Common:4; Rare:112 | ||||
| chr16:8621585-8621771 | Common:1; Rare:73 | ||||
| chr16:8674419-8674681 | Common:1; Rare:90; Clinvar:2 | ||||
| chr16:8720537-8720822 | Common:2; Rare:81 | ||||
| chr16:8797625-8797885 | Rare:103; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8861680-8861829 | Common:1; Rare:50 | ||||
| chr16:8868971-8869261 | Common:4; Rare:128 | ||||
| chr16:8935796-8935911 | Rare:31 | ||||
| chr16:8962584-8962755 | Common:2; Rare:58 |