| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67404717-67405103 | Rare:67 | ||||
| chr16:67430507-67430677 | Rare:27 | ||||
| chr16:67430760-67431168 | Common:3; Rare:79 | ||||
| chr16:67431280-67431403 | Rare:29; Clinvar (pathogenic):1 | ||||
| chr16:67431404-67431488 | Rare:22 | ||||
| chr16:67480498-67480734 | Rare:36 | ||||
| chr16:67480826-67480902 | Rare:11 | ||||
| chr16:67481099-67481475 | Common:2; Rare:126 | ||||
| chr16:67527846-67527991 | Common:1; Rare:30 | ||||
| chr16:67528697-67528961 | Rare:66 | ||||
| chr16:67529548-67529770 | Rare:44 | ||||
| chr16:67530205-67530544 | Common:1; Rare:70 | ||||
| chr16:67537375-67537535 | Common:2; Rare:28 | ||||
| chr16:67537753-67537773 | Rare:6 | ||||
| chr16:67537840-67538267 | Common:5; Rare:110 |