| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23202930-23203213 | Common:1; Rare:98 | ||||
| chr3:23805855-23806088 | Common:1; Rare:48 | ||||
| chr3:23916801-23917354 | Rare:186 | ||||
| chr3:23917585-23917990 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr3:25428107-25428408 | Rare:67 | ||||
| chr3:25783371-25783617 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr3:25789993-25790126 | Common:4; Rare:51 | ||||
| chr3:26622707-26622778 | Rare:17 | ||||
| chr3:26623768-26623886 | Common:1; Rare:20 | ||||
| chr3:27369313-27369568 | Rare:55 | ||||
| chr3:28241461-28241788 | Common:2; Rare:115 | ||||
| chr3:28348471-28348721 | Common:1; Rare:53 | ||||
| chr3:28348779-28349196 | Common:4; Rare:132 | ||||
| chr3:29280822-29281389 | Common:15; Rare:111 | ||||
| chr3:31981619-31981875 | Common:1; Rare:61 |