| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8868937-8869322 | Common:6; Rare:172 | ||||
| chr16:8898881-8899126 | Common:4; Rare:66 | ||||
| chr16:8962426-8962492 | Rare:20 | ||||
| chr16:8962572-8962895 | Common:4; Rare:106 | ||||
| chr16:8963793-8964178 | Common:3; Rare:142 | ||||
| chr16:9091063-9091243 | Rare:67 | ||||
| chr16:9091322-9091763 | Common:1; Rare:171 | ||||
| chr16:9092251-9092618 | Common:2; Rare:145 | ||||
| chr16:10386014-10386171 | Common:1; Rare:57 | ||||
| chr16:10743711-10743893 | Rare:76 | ||||
| chr16:10743962-10744367 | Common:2; Rare:174 | ||||
| chr16:10775514-10775666 | Rare:32 | ||||
| chr16:10876810-10876839 | Rare:4 | ||||
| chr16:10876850-10877308 | Common:2; Rare:98; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:10877567-10877660 | Common:2; Rare:27 |