| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189784276-189784543 | Common:4; Rare:97; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190534688-190534913 | Common:1; Rare:72 | ||||
| chr2:190880626-190880881 | Common:4; Rare:86 | ||||
| chr2:191014133-191014333 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245247-191245535 | Common:2; Rare:92 | ||||
| chr2:191677841-191678208 | Common:4; Rare:103 | ||||
| chr2:191678565-191678591 | Rare:13 | ||||
| chr2:197434973-197435227 | Rare:83 | ||||
| chr2:197453239-197453563 | Rare:112 | ||||
| chr2:197499783-197500430 | Common:2; Rare:246; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515827-197516087 | Common:2; Rare:96 | ||||
| chr2:199911104-199911409 | Rare:98 | ||||
| chr2:200509883-200510199 | Common:1; Rare:110 | ||||
| chr2:200585867-200586103 | Rare:61 | ||||
| chr2:200609135-200609381 | Rare:61 |