| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15094247-15094389 | Rare:71 | ||||
| chr16:15857019-15857142 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr16:18801588-18801896 | Common:2; Rare:87 | ||||
| chr16:19067422-19067696 | Common:5; Rare:111; Clinvar:1 | ||||
| chr16:19067773-19067920 | Common:2; Rare:35 | ||||
| chr16:19521995-19522145 | Rare:43 | ||||
| chr16:20763931-20764056 | Common:2; Rare:21 | ||||
| chr16:20806349-20806610 | Rare:89 | ||||
| chr16:22092267-22092550 | Rare:48 | ||||
| chr16:22437189-22437296 | Rare:34 | ||||
| chr16:23452733-23452795 | Rare:20 | ||||
| chr16:23453163-23453265 | Rare:30 | ||||
| chr16:23557336-23557472 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641257-23641530 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:24729611-24729739 | Common:6; Rare:69 |