| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148021490-148021632 | Rare:36 | ||||
| chr2:149587310-149587372 | Rare:11 | ||||
| chr2:152717821-152718029 | Rare:82 | ||||
| chr2:152718453-152718644 | Rare:70 | ||||
| chr2:159712340-159712571 | Common:2; Rare:87 | ||||
| chr2:162243379-162243669 | Common:1; Rare:50 | ||||
| chr2:162318650-162318841 | Common:1; Rare:39 | ||||
| chr2:169584744-169584821 | Rare:20 | ||||
| chr2:169694383-169694571 | Common:5; Rare:53 | ||||
| chr2:171433976-171434342 | Common:2; Rare:97 | ||||
| chr2:172427346-172427687 | Common:9; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:173965232-173965518 | Common:1; Rare:100 | ||||
| chr2:174395629-174395806 | Common:1; Rare:58 | ||||
| chr2:176188528-176188668 | Common:1; Rare:51 | ||||
| chr2:177392643-177392792 | Common:1; Rare:36; Clinvar:1 |