| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4734125-4734298 | Common:1; Rare:61 | ||||
| chr16:4767126-4767321 | Common:1; Rare:64 | ||||
| chr16:4847231-4847672 | Common:3; Rare:198 | ||||
| chr16:5033920-5033968 | Rare:19 | ||||
| chr16:5097728-5098015 | Common:4; Rare:102 | ||||
| chr16:8621575-8621745 | Common:1; Rare:63 | ||||
| chr16:8797612-8797885 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868983-8869251 | Common:4; Rare:119 | ||||
| chr16:8962528-8962755 | Common:3; Rare:81 | ||||
| chr16:9092162-9092270 | Rare:33 | ||||
| chr16:10385713-10386089 | Rare:130 | ||||
| chr16:10743746-10743880 | Rare:53 | ||||
| chr16:10744061-10744163 | Rare:44 | ||||
| chr16:10877004-10877358 | Common:2; Rare:84; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:10878626-10879032 | Rare:91 |