| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4467237-4467325 | Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493151-4493526 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:5187327-5187635 | Common:5; Rare:121 | ||||
| chr3:8501620-8501937 | Common:2; Rare:120 | ||||
| chr3:9249617-9249757 | Common:1; Rare:36 | ||||
| chr3:9362912-9363279 | Common:5; Rare:100 | ||||
| chr3:9363310-9363420 | Rare:20 | ||||
| chr3:9397418-9397891 | Common:1; Rare:152 | ||||
| chr3:9749829-9750088 | Common:1; Rare:80 | ||||
| chr3:9750135-9750362 | Common:1; Rare:79 | ||||
| chr3:9792243-9792584 | Common:1; Rare:90 | ||||
| chr3:9792618-9792652 | Rare:11 | ||||
| chr3:9792676-9793148 | Common:3; Rare:169 | ||||
| chr3:9843968-9844141 | Common:2; Rare:69 | ||||
| chr3:9890507-9890690 | Common:2; Rare:69 |