| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46693660-46693823 | Common:1; Rare:39 | ||||
| chr3:46882092-46882264 | Common:1; Rare:51 | ||||
| chr3:46979486-46979846 | Common:2; Rare:86; Clinvar:1 | ||||
| chr3:47163884-47164260 | Common:1; Rare:107; Clinvar (pathogenic):1 | ||||
| chr3:47380780-47381090 | Rare:104 | ||||
| chr3:47381436-47381508 | Rare:19 | ||||
| chr3:47475797-47476084 | Common:3; Rare:112 | ||||
| chr3:47513345-47513511 | Common:1; Rare:45 | ||||
| chr3:47513633-47513788 | Common:1; Rare:49 | ||||
| chr3:47781682-47782012 | Rare:118 | ||||
| chr3:47802851-47803208 | Common:1; Rare:111 | ||||
| chr3:48088782-48089092 | Rare:105 | ||||
| chr3:48089248-48089363 | Rare:34 | ||||
| chr3:48301321-48301449 | Common:1; Rare:41 | ||||
| chr3:48301528-48301622 | Common:1; Rare:28 |