| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:164841202-164841520 | Rare:90 | ||||
| chr2:164841805-164841895 | Common:1; Rare:22 | ||||
| chr2:164955249-164955658 | Rare:95 | ||||
| chr2:165794247-165794317 | Rare:28; Clinvar:2 | ||||
| chr2:165794594-165794972 | Common:1; Rare:70 | ||||
| chr2:166375877-166376306 | Common:5; Rare:111; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:168890361-168890552 | Common:2; Rare:47 | ||||
| chr2:169478628-169478795 | Common:2; Rare:20 | ||||
| chr2:169479357-169479556 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr2:169584290-169584630 | Common:1; Rare:129 | ||||
| chr2:169584692-169584825 | Rare:37 | ||||
| chr2:169694369-169694575 | Common:5; Rare:64 | ||||
| chr2:170928989-170929331 | Common:4; Rare:112 | ||||
| chr2:171160294-171160586 | Rare:108 | ||||
| chr2:171433917-171434343 | Common:3; Rare:115 |