| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177552761-177552841 | Common:1; Rare:29 | ||||
| chr2:177618706-177618837 | Common:1; Rare:39 | ||||
| chr2:178072745-178072885 | Rare:36 | ||||
| chr2:178194349-178194521 | Common:1; Rare:60 | ||||
| chr2:178450731-178450868 | Rare:47 | ||||
| chr2:178451090-178451382 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478514-178478644 | Common:1; Rare:41 | ||||
| chr2:178480192-178480365 | Common:1; Rare:54 | ||||
| chr2:178651418-178651466 | Rare:20; Clinvar (benign):1 | ||||
| chr2:178807031-178807504 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:179264508-179264861 | Common:4; Rare:132 | ||||
| chr2:180980258-180980545 | Common:1; Rare:90 | ||||
| chr2:181891664-181892111 | Common:4; Rare:181 | ||||
| chr2:182426979-182427072 | Rare:21 | ||||
| chr2:182716094-182716426 | Common:2; Rare:112 |