| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:65056133-65056348 | Rare:63 | ||||
| chr2:65227597-65227955 | Rare:95 | ||||
| chr2:68157504-68157957 | Common:2; Rare:231 | ||||
| chr2:68252483-68252834 | Common:3; Rare:109 | ||||
| chr2:68365135-68365390 | Common:2; Rare:47 | ||||
| chr2:68387459-68387780 | Common:1; Rare:40 | ||||
| chr2:68467255-68467605 | Common:2; Rare:91 | ||||
| chr2:69387207-69387436 | Rare:71; Clinvar:2 | ||||
| chr2:69829472-69829737 | Common:1; Rare:107 | ||||
| chr2:69914758-69915165 | Common:1; Rare:103 | ||||
| chr2:70087305-70087494 | Common:2; Rare:69 | ||||
| chr2:70087555-70088037 | Rare:149 | ||||
| chr2:70293675-70293852 | Common:3; Rare:54 | ||||
| chr2:71068523-71068732 | Rare:89 | ||||
| chr2:71130225-71130685 | Common:6; Rare:134; Clinvar:1; Clinvar (benign):2 |