| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176188524-176188668 | Common:1; Rare:51 | ||||
| chr2:176269369-176269505 | Common:1; Rare:55 | ||||
| chr2:177212416-177212857 | Common:4; Rare:172 | ||||
| chr2:177263402-177263687 | Common:1; Rare:68 | ||||
| chr2:177263738-177264151 | Common:2; Rare:112 | ||||
| chr2:177264533-177264826 | Common:2; Rare:85 | ||||
| chr2:177392651-177393070 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552755-177552838 | Common:1; Rare:31 | ||||
| chr2:177618699-177618784 | Common:1; Rare:35 | ||||
| chr2:178072708-178072884 | Rare:45 | ||||
| chr2:178450713-178450901 | Common:1; Rare:68 | ||||
| chr2:178451090-178451382 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478504-178478671 | Common:1; Rare:53 | ||||
| chr2:178480175-178480510 | Common:2; Rare:96 | ||||
| chr2:179264503-179264861 | Common:4; Rare:133 |