| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30069565-30070029 | Common:1; Rare:174; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30075887-30076055 | Rare:56 | ||||
| chr16:30091885-30092104 | Common:1; Rare:51 | ||||
| chr16:30095122-30095413 | Common:1; Rare:86 | ||||
| chr16:30096097-30096412 | Rare:87 | ||||
| chr16:30096895-30097094 | Rare:31 | ||||
| chr16:30123043-30123371 | Common:6; Rare:94 | ||||
| chr16:30183508-30183724 | Common:2; Rare:44 | ||||
| chr16:30184528-30184759 | Common:1; Rare:41 | ||||
| chr16:30193654-30193913 | |||||
| chr16:30355211-30355438 | Common:1; Rare:79 | ||||
| chr16:30355846-30355947 | Common:1; Rare:24 | ||||
| chr16:30445834-30446030 | Common:1; Rare:61 | ||||
| chr16:30472570-30472832 | Rare:50 | ||||
| chr16:30483838-30484136 | Common:1; Rare:72 |