| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:6019751-6019931 | Rare:67; Clinvar:1 | ||||
| chr16:8621608-8621757 | Common:1; Rare:57 | ||||
| chr16:8674372-8674654 | Common:1; Rare:100; Clinvar:2 | ||||
| chr16:8797567-8797900 | Common:3; Rare:139; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868973-8869311 | Common:6; Rare:151 | ||||
| chr16:10580567-10580756 | Rare:58 | ||||
| chr16:10743740-10743855 | Rare:40 | ||||
| chr16:10744061-10744301 | Common:1; Rare:88 | ||||
| chr16:10818576-10818709 | Common:1; Rare:41 | ||||
| chr16:10944326-10944630 | Common:1; Rare:93 | ||||
| chr16:11345261-11345451 | Common:1; Rare:66 | ||||
| chr16:11668195-11668510 | Common:3; Rare:134 | ||||
| chr16:11797143-11797499 | Common:2; Rare:134 | ||||
| chr16:11851482-11851677 | Common:1; Rare:103 | ||||
| chr16:11915889-11916238 | Common:2; Rare:139 |