| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144519267-144519433 | Rare:19 | ||||
| chr2:152390636-152390741 | Common:2; Rare:17 | ||||
| chr2:156334478-156334790 | Rare:68 | ||||
| chr2:159780124-159780324 | Rare:61 | ||||
| chr2:168138363-168138735 | Common:2; Rare:71 | ||||
| chr2:169811022-169811323 | Rare:89 | ||||
| chr2:170751570-170751709 | Common:1; Rare:18 | ||||
| chr2:170770789-170771090 | Common:2; Rare:50 | ||||
| chr2:176637582-176637762 | Common:3; Rare:65 | ||||
| chr2:177234163-177234454 | Rare:68; Clinvar:2 | ||||
| chr2:178413908-178413994 | Rare:26 | ||||
| chr2:178576812-178576951 | Rare:32; Clinvar (benign):3 | ||||
| chr2:178612099-178612416 | Rare:94; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr2:178689093-178689269 | Common:1; Rare:40; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:197488463-197488590 | Common:2; Rare:22; Clinvar:1; Clinvar (benign):1 |