| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30876103-30876249 | Common:1; Rare:22 | ||||
| chr16:30876473-30876618 | Rare:24 | ||||
| chr16:30902220-30902367 | Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:30902481-30902614 | Rare:48; Clinvar:6 | ||||
| chr16:30902771-30902788 | Rare:5; Clinvar:1 | ||||
| chr16:30950016-30950285 | Rare:46 | ||||
| chr16:30995282-30995531 | Common:2; Rare:39 | ||||
| chr16:30995805-30995930 | Rare:22 | ||||
| chr16:30995965-30996283 | Rare:52 | ||||
| chr16:30996305-30996518 | Rare:27 | ||||
| chr16:31476965-31477126 | Rare:50 | ||||
| chr16:31700396-31700670 | Common:4; Rare:62 | ||||
| chr16:31700904-31701227 | Common:2; Rare:36 | ||||
| chr16:31870917-31871058 | Rare:21 | ||||
| chr16:31874568-31874776 | Rare:37 |