| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47513353-47513525 | Common:1; Rare:52 | ||||
| chr3:47781682-47782061 | Common:1; Rare:146 | ||||
| chr3:48088781-48089065 | Rare:92 | ||||
| chr3:48089239-48089325 | Rare:28 | ||||
| chr3:48301330-48301449 | Common:1; Rare:37 | ||||
| chr3:48301539-48301622 | Common:1; Rare:24 | ||||
| chr3:48440035-48440347 | Common:1; Rare:127 | ||||
| chr3:48446622-48446743 | Rare:43 | ||||
| chr3:48473010-48473177 | Common:1; Rare:34 | ||||
| chr3:48473181-48473441 | Common:1; Rare:50 | ||||
| chr3:48504062-48504302 | Common:2; Rare:77 | ||||
| chr3:48556752-48557173 | Common:1; Rare:103 | ||||
| chr3:48635407-48635613 | Rare:68 | ||||
| chr3:48847663-48847973 | Common:1; Rare:86 | ||||
| chr3:48898797-48899062 | Rare:80; Clinvar:7; Clinvar (benign):1 |