| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:193593101-193593338 | Rare:72; Clinvar:1 | ||||
| chr3:194633654-194633793 | Common:3; Rare:27 | ||||
| chr3:196287664-196288027 | Common:2; Rare:112 | ||||
| chr3:196318179-196318374 | Common:1; Rare:81 | ||||
| chr3:196503655-196503945 | Common:5; Rare:101 | ||||
| chr3:196568518-196568663 | Common:3; Rare:37 | ||||
| chr3:196639622-196639793 | Rare:39 | ||||
| chr3:196712220-196712324 | Common:2; Rare:34 | ||||
| chr3:196867770-196867946 | Rare:63 | ||||
| chr3:196942388-196942604 | Rare:90 | ||||
| chr3:197736838-197737148 | Common:3; Rare:103 | ||||
| chr3:197749821-197750004 | Rare:72 | ||||
| chr3:197791216-197791290 | Common:1; Rare:36 | ||||
| chr3:197949885-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959989-197960248 | Common:1; Rare:91 |