| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15949486-15949646 | Common:1; Rare:46 | ||||
| chr16:18790237-18790467 | Common:4; Rare:83 | ||||
| chr16:18801482-18801830 | Common:4; Rare:121 | ||||
| chr16:19067455-19067678 | Common:5; Rare:85; Clinvar:1 | ||||
| chr16:19113774-19113940 | Common:1; Rare:32 | ||||
| chr16:19718517-19718573 | Rare:20 | ||||
| chr16:20763942-20764056 | Common:1; Rare:21 | ||||
| chr16:20806377-20806619 | Rare:87 | ||||
| chr16:21233592-21233727 | Rare:29 | ||||
| chr16:21599362-21599676 | Common:4; Rare:111 | ||||
| chr16:21599710-21599761 | Rare:12 | ||||
| chr16:21952991-21953445 | Common:1; Rare:115; Clinvar (benign):3 | ||||
| chr16:21962180-21962515 | Rare:58; Clinvar (pathogenic):1 | ||||
| chr16:22008009-22008313 | Common:1; Rare:96 | ||||
| chr16:22206018-22206326 | Common:1; Rare:83 |