| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176188538-176188668 | Common:1; Rare:50 | ||||
| chr2:177212422-177212831 | Common:4; Rare:162 | ||||
| chr2:177263427-177263682 | Common:1; Rare:61 | ||||
| chr2:177264563-177264813 | Common:2; Rare:72 | ||||
| chr2:177392651-177393070 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552768-177552855 | Common:1; Rare:26 | ||||
| chr2:178451090-178451317 | Common:5; Rare:69; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478464-178478711 | Common:1; Rare:75 | ||||
| chr2:179264508-179264898 | Common:4; Rare:147 | ||||
| chr2:180980246-180980545 | Common:1; Rare:94 | ||||
| chr2:181891665-181892231 | Common:6; Rare:214 | ||||
| chr2:182426712-182426895 | Rare:34 | ||||
| chr2:182427007-182427122 | Rare:22 | ||||
| chr2:182715941-182716355 | Common:3; Rare:142 | ||||
| chr2:186485931-186486364 | Common:3; Rare:121 |