| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:63911923-63912116 | Rare:57 | ||||
| chr3:66038410-66038661 | Rare:56 | ||||
| chr3:66038748-66038938 | Common:2; Rare:67 | ||||
| chr3:67654556-67654795 | Common:2; Rare:93 | ||||
| chr3:69013590-69013750 | Rare:42 | ||||
| chr3:69084762-69085079 | Common:3; Rare:80 | ||||
| chr3:71130527-71130899 | Common:1; Rare:105; Clinvar:2 | ||||
| chr3:72996709-72997051 | Common:2; Rare:126 | ||||
| chr3:77039786-77040115 | Common:3; Rare:107 | ||||
| chr3:79018811-79018991 | Common:1; Rare:43 | ||||
| chr3:79018999-79019046 | Rare:17 | ||||
| chr3:81761503-81761735 | Common:8; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:81761738-81761950 | Rare:54 | ||||
| chr3:87227032-87227497 | Common:3; Rare:138; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058536-88058723 | Common:1; Rare:61 |