| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:677358-677549 | Common:1; Rare:82 | ||||
| chr2:3519483-3519623 | Common:2; Rare:51 | ||||
| chr2:3558220-3558695 | Common:6; Rare:179 | ||||
| chr2:3575092-3575358 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:6877593-6877779 | Common:2; Rare:36 | ||||
| chr2:9423163-9423302 | Common:1; Rare:30 | ||||
| chr2:9423393-9423709 | Rare:100 | ||||
| chr2:9474484-9474630 | Common:6; Rare:64 | ||||
| chr2:9555712-9555992 | Common:2; Rare:95 | ||||
| chr2:10689898-10689989 | Common:2; Rare:36 | ||||
| chr2:11466118-11466318 | Common:4; Rare:49 | ||||
| chr2:11746402-11746648 | Common:1; Rare:67; Clinvar:2 | ||||
| chr2:17753721-17754195 | Common:5; Rare:149; Clinvar (benign):1 | ||||
| chr2:19901668-19901798 | Common:1; Rare:71 | ||||
| chr2:19901948-19902051 | Common:1; Rare:34 |