| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67806441-67806906 | Rare:111 | ||||
| chr16:67806958-67807120 | Rare:53 | ||||
| chr16:67833800-67834038 | Common:1; Rare:91 | ||||
| chr16:67841794-67842116 | Common:1; Rare:94 | ||||
| chr16:67842204-67842403 | Rare:59 | ||||
| chr16:67842566-67842686 | Rare:22 | ||||
| chr16:67842783-67843154 | Common:7; Rare:214; Clinvar (pathogenic):1 | ||||
| chr16:67846661-67847040 | Common:1; Rare:101 | ||||
| chr16:67847112-67847223 | Rare:26 | ||||
| chr16:67847631-67847684 | Rare:10 | ||||
| chr16:67872939-67873223 | Rare:87 | ||||
| chr16:67873421-67873437 | Rare:5 | ||||
| chr16:67884726-67884906 | Rare:54 | ||||
| chr16:67892933-67893370 | Common:7; Rare:126 | ||||
| chr16:67893443-67893527 | Rare:20 |