| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15094247-15094409 | Rare:77 | ||||
| chr16:15395906-15396014 | Rare:38 | ||||
| chr16:15643034-15643267 | Rare:72 | ||||
| chr16:15856946-15857142 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:15857295-15857347 | Rare:13 | ||||
| chr16:18801440-18801796 | Common:2; Rare:123 | ||||
| chr16:19067441-19067696 | Common:5; Rare:105; Clinvar:1 | ||||
| chr16:19067791-19067941 | Common:2; Rare:37 | ||||
| chr16:19113706-19113969 | Common:1; Rare:47 | ||||
| chr16:19522011-19522214 | Rare:50 | ||||
| chr16:20674658-20674775 | Common:2; Rare:29 | ||||
| chr16:20676200-20676241 | Common:1; Rare:11 | ||||
| chr16:20741740-20742142 | Common:1; Rare:137 | ||||
| chr16:20763937-20764021 | Common:2; Rare:14 | ||||
| chr16:20806349-20806546 | Rare:73 |