| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27427054-27427312 | Common:2; Rare:49 | ||||
| chr16:27549808-27550230 | Common:2; Rare:164 | ||||
| chr16:28211159-28211308 | Common:2; Rare:43 | ||||
| chr16:28211844-28212357 | Common:5; Rare:170 | ||||
| chr16:28491354-28491554 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:28492067-28492254 | Rare:42; Clinvar:3 | ||||
| chr16:28494043-28494389 | Common:3; Rare:61 | ||||
| chr16:28506808-28506927 | Rare:33 | ||||
| chr16:28553903-28554028 | Common:3; Rare:40 | ||||
| chr16:28554079-28554391 | Common:5; Rare:120 | ||||
| chr16:28822485-28822836 | Common:1; Rare:117 | ||||
| chr16:28822848-28823191 | Common:3; Rare:109 | ||||
| chr16:28823654-28823711 | Common:1; Rare:13 | ||||
| chr16:28823739-28824194 | Common:3; Rare:137 | ||||
| chr16:28845480-28845620 | Common:2; Rare:39 |