| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30650774-30651015 | Rare:79 | ||||
| chr16:30697954-30698270 | Common:1; Rare:141 | ||||
| chr16:30698467-30698653 | Common:1; Rare:73 | ||||
| chr16:30699050-30699598 | Common:1; Rare:135; Clinvar (benign):1 | ||||
| chr16:30748125-30748448 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30761446-30761532 | Rare:30 | ||||
| chr16:30762044-30762322 | Common:3; Rare:93 | ||||
| chr16:30765217-30765475 | Rare:74 | ||||
| chr16:30893972-30894307 | Common:5; Rare:86 | ||||
| chr16:30896458-30896662 | Common:1; Rare:49 | ||||
| chr16:30923227-30923601 | Common:1; Rare:89 | ||||
| chr16:30957009-30957302 | Common:3; Rare:64 | ||||
| chr16:30957624-30957757 | Common:1; Rare:40 | ||||
| chr16:30984935-30985277 | Common:1; Rare:88 | ||||
| chr16:31033279-31033847 | Common:2; Rare:160 |