| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38751339-38751531 | Common:2; Rare:90 | ||||
| chr2:38875667-38875825 | Common:1; Rare:39 | ||||
| chr2:38875886-38876109 | Common:1; Rare:81 | ||||
| chr2:38876365-38876479 | Common:1; Rare:26 | ||||
| chr2:39007175-39007406 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:39007431-39007553 | Common:3; Rare:28; Clinvar (benign):1 | ||||
| chr2:39023792-39024069 | Rare:56; Clinvar (benign):2 | ||||
| chr2:39120995-39121067 | Rare:23 | ||||
| chr2:39124286-39124427 | Rare:51 | ||||
| chr2:39436995-39437485 | Common:5; Rare:181 | ||||
| chr2:39779160-39779392 | Common:4; Rare:82 | ||||
| chr2:42169156-42169635 | Common:3; Rare:220 | ||||
| chr2:42425063-42425176 | Rare:24 | ||||
| chr2:42792535-42792754 | Common:2; Rare:66 | ||||
| chr2:43595908-43596216 | Common:1; Rare:108 |