| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:156332714-156332870 | Rare:48; Clinvar:2 | ||||
| chr2:158968416-158968700 | Rare:90 | ||||
| chr2:159286622-159286912 | Common:5; Rare:110 | ||||
| chr2:159516517-159516669 | Common:1; Rare:17 | ||||
| chr2:159615534-159615671 | Common:1; Rare:47 | ||||
| chr2:159712358-159712571 | Common:2; Rare:84 | ||||
| chr2:160271308-160271573 | Rare:54 | ||||
| chr2:161308384-161308508 | Common:2; Rare:29 | ||||
| chr2:162343873-162344217 | Common:1; Rare:113 | ||||
| chr2:164840493-164840815 | Common:1; Rare:56 | ||||
| chr2:164841192-164841550 | Rare:103 | ||||
| chr2:164841805-164841971 | Common:1; Rare:46 | ||||
| chr2:164842175-164842244 | Common:1; Rare:12 | ||||
| chr2:165794122-165794323 | Common:2; Rare:57; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:169584303-169584622 | Common:1; Rare:122 |