| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75710462-75710760 | Common:2; Rare:99 | ||||
| chr2:75710852-75710974 | Common:1; Rare:47 | ||||
| chr2:79025635-79025787 | Rare:29 | ||||
| chr2:79292861-79292970 | Rare:24 | ||||
| chr2:79512650-79513099 | Common:2; Rare:145 | ||||
| chr2:84459219-84459615 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84516279-84516571 | Common:1; Rare:78 | ||||
| chr2:84905459-84905831 | Common:2; Rare:117 | ||||
| chr2:84905835-84906116 | Common:1; Rare:65 | ||||
| chr2:84906957-84907132 | Common:1; Rare:25 | ||||
| chr2:85327916-85328094 | Common:3; Rare:80 | ||||
| chr2:85354501-85354866 | Common:2; Rare:118 | ||||
| chr2:85413992-85414074 | Common:1; Rare:22 | ||||
| chr2:85418405-85418784 | Common:5; Rare:99 | ||||
| chr2:85420791-85420922 | Common:2; Rare:31 |