| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:163735992-163736106 | Rare:21 | ||||
| chr2:164840383-164840756 | Common:1; Rare:61 | ||||
| chr2:164841232-164841562 | Rare:97 | ||||
| chr2:164841796-164841900 | Common:1; Rare:25 | ||||
| chr2:164842190-164842265 | Common:1; Rare:17 | ||||
| chr2:164955478-164955645 | Rare:39 | ||||
| chr2:165469561-165469711 | Rare:27 | ||||
| chr2:165794122-165794323 | Common:2; Rare:57; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:169479382-169479565 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr2:169584734-169584812 | Rare:17 | ||||
| chr2:169694360-169694571 | Common:5; Rare:67 | ||||
| chr2:170928917-170929313 | Common:4; Rare:115 | ||||
| chr2:171160352-171160469 | Rare:44 | ||||
| chr2:171433955-171434234 | Common:2; Rare:71 | ||||
| chr2:171894217-171894330 | Rare:55; Clinvar:1 |