| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176188497-176188668 | Common:1; Rare:66 | ||||
| chr2:177212416-177212821 | Common:4; Rare:164 | ||||
| chr2:177231832-177232180 | Common:2; Rare:81 | ||||
| chr2:177263419-177263682 | Common:1; Rare:62 | ||||
| chr2:177263809-177263852 | Rare:13 | ||||
| chr2:177264048-177264177 | Rare:42 | ||||
| chr2:177264540-177264793 | Common:2; Rare:70 | ||||
| chr2:177392644-177393070 | Common:3; Rare:145; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552828 | Rare:27 | ||||
| chr2:177618699-177619010 | Common:7; Rare:85 | ||||
| chr2:178450731-178450881 | Rare:50 | ||||
| chr2:178451090-178451382 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:179264501-179264861 | Common:4; Rare:133 | ||||
| chr2:180980246-180980545 | Common:1; Rare:94 | ||||
| chr2:181458040-181458230 | Rare:58 |