| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150408539-150408667 | Rare:41 | ||||
| chr3:150567754-150567934 | Common:1; Rare:47 | ||||
| chr3:150603153-150603328 | Common:1; Rare:66 | ||||
| chr3:152268848-152269095 | Rare:89 | ||||
| chr3:152269501-152269752 | Common:2; Rare:76 | ||||
| chr3:155079425-155079713 | Common:6; Rare:69 | ||||
| chr3:155854364-155854778 | Rare:117 | ||||
| chr3:156554988-156555321 | Common:1; Rare:133 | ||||
| chr3:156674442-156674631 | Common:1; Rare:51 | ||||
| chr3:157160103-157160327 | Rare:95 | ||||
| chr3:157436770-157437009 | Common:2; Rare:55 | ||||
| chr3:158644338-158644677 | Common:5; Rare:109; Clinvar (benign):6 | ||||
| chr3:158732155-158732242 | Common:2; Rare:26 | ||||
| chr3:158732419-158732705 | Common:3; Rare:95 | ||||
| chr3:158732744-158732968 | Rare:31 |