| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:63588703-63589025 | Rare:101 | ||||
| chr2:63840819-63841164 | Common:2; Rare:97 | ||||
| chr2:63841705-63841921 | Common:1; Rare:78 | ||||
| chr2:64144323-64144683 | Common:4; Rare:105 | ||||
| chr2:64524067-64524448 | Common:3; Rare:124 | ||||
| chr2:65056160-65056462 | Common:2; Rare:103 | ||||
| chr2:65227579-65227877 | Rare:86 | ||||
| chr2:66434802-66435297 | Common:2; Rare:117 | ||||
| chr2:68157456-68157949 | Common:2; Rare:253 | ||||
| chr2:68252175-68252350 | Common:2; Rare:53 | ||||
| chr2:68252523-68252898 | Common:3; Rare:125 | ||||
| chr2:68319692-68319820 | Rare:35 | ||||
| chr2:68467292-68467594 | Common:1; Rare:72 | ||||
| chr2:69387172-69387373 | Rare:51; Clinvar:2 | ||||
| chr2:69437404-69437544 | Rare:66; Clinvar:2; Clinvar (benign):2 |