| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:190862653-190862863 | Rare:57 | ||||
| chr3:191329551-191329632 | Common:2; Rare:20 | ||||
| chr3:193593095-193593303 | Rare:65; Clinvar:1 | ||||
| chr3:194672153-194672471 | Common:1; Rare:96 | ||||
| chr3:195543210-195543475 | Common:3; Rare:100 | ||||
| chr3:195583878-195584405 | Common:12; Rare:107 | ||||
| chr3:196287677-196287821 | Common:1; Rare:45 | ||||
| chr3:196318184-196318350 | Common:1; Rare:68 | ||||
| chr3:196639604-196639805 | Common:2; Rare:48 | ||||
| chr3:196712208-196712316 | Common:1; Rare:37 | ||||
| chr3:196867770-196867946 | Rare:63 | ||||
| chr3:196942390-196942640 | Common:1; Rare:100 | ||||
| chr3:197029780-197029917 | Common:1; Rare:45 | ||||
| chr3:197736833-197737133 | Common:3; Rare:95 | ||||
| chr3:197949875-197950250 | Common:4; Rare:112; Clinvar (benign):2 |