| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69339461-69339893 | Common:2; Rare:188; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:69340031-69340091 | Rare:25 | ||||
| chr16:69351773-69351938 | Rare:32 | ||||
| chr16:69385600-69386167 | Rare:169 | ||||
| chr16:69424295-69424815 | Common:3; Rare:144 | ||||
| chr16:69425205-69425283 | Common:1; Rare:19 | ||||
| chr16:69565589-69566121 | Common:6; Rare:189 | ||||
| chr16:69566215-69566395 | Common:1; Rare:53 | ||||
| chr16:69566487-69566691 | Rare:47 | ||||
| chr16:69566836-69566976 | Rare:24 | ||||
| chr16:69726369-69726877 | Common:5; Rare:147 | ||||
| chr16:69726982-69727129 | Rare:30 | ||||
| chr16:69754642-69754717 | Rare:25 | ||||
| chr16:69754781-69755209 | Common:1; Rare:147 | ||||
| chr16:69762168-69762635 | Common:3; Rare:156 |