| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:161340089-161340397 | Common:2; Rare:58 | ||||
| chr2:162317901-162318031 | Rare:51; Clinvar:1 | ||||
| chr2:164535436-164535560 | Common:1; Rare:20 | ||||
| chr2:164644528-164644785 | Rare:39 | ||||
| chr2:165749838-165750146 | Common:1; Rare:74 | ||||
| chr2:168457061-168457064 | Rare:1 | ||||
| chr2:169231725-169232042 | Common:4; Rare:83; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:169363560-169363716 | Common:1; Rare:28 | ||||
| chr2:169811074-169811215 | Rare:37 | ||||
| chr2:170770772-170771132 | Common:3; Rare:63 | ||||
| chr2:171517321-171517493 | Common:1; Rare:46 | ||||
| chr2:171524178-171524320 | Common:6; Rare:22 | ||||
| chr2:172484614-172484903 | Rare:51 | ||||
| chr2:172995578-172995587 | Common:1; Rare:1 | ||||
| chr2:175167357-175167607 | Rare:61 |