| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38376222-38376461 | Common:1; Rare:71 | ||||
| chr2:38376807-38376964 | Common:1; Rare:56 | ||||
| chr2:38377093-38377640 | Common:3; Rare:230 | ||||
| chr2:38602040-38602443 | Common:6; Rare:146 | ||||
| chr2:38602688-38603308 | Common:7; Rare:234 | ||||
| chr2:38665831-38666193 | Common:3; Rare:102 | ||||
| chr2:38666340-38666431 | Rare:30 | ||||
| chr2:38750806-38750944 | Common:2; Rare:55 | ||||
| chr2:38751085-38751687 | Common:7; Rare:281 | ||||
| chr2:38751869-38751995 | Common:3; Rare:35 | ||||
| chr2:38778099-38778253 | Rare:39 | ||||
| chr2:38875563-38876080 | Common:3; Rare:151 | ||||
| chr2:39120200-39120302 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr2:39120362-39120642 | Common:1; Rare:112; Clinvar:2; Clinvar (benign):6 | ||||
| chr2:39120678-39121486 | Common:4; Rare:256 |