| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74421603-74421779 | Rare:57 | ||||
| chr2:74465343-74465457 | Common:1; Rare:31; Clinvar:1 | ||||
| chr2:74529642-74530041 | Rare:127; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74553907-74554151 | Rare:49 | ||||
| chr2:74958776-74959087 | Rare:116 | ||||
| chr2:75710864-75711203 | Common:2; Rare:95 | ||||
| chr2:84905523-84905683 | Common:1; Rare:49 | ||||
| chr2:85354550-85354807 | Common:1; Rare:80 | ||||
| chr2:85539019-85539355 | Common:3; Rare:168; Clinvar (benign):7 | ||||
| chr2:85561424-85561568 | Rare:52; Clinvar:4 | ||||
| chr2:85595565-85595769 | Common:1; Rare:66 | ||||
| chr2:85602620-85602909 | Rare:75 | ||||
| chr2:85612027-85612103 | Rare:20 | ||||
| chr2:85888869-85889189 | Common:3; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:86105861-86105905 | Rare:13 |