| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:181891651-181892074 | Common:4; Rare:173 | ||||
| chr2:182715935-182716345 | Common:3; Rare:141 | ||||
| chr2:183124249-183124443 | Common:4; Rare:63 | ||||
| chr2:186485987-186486344 | Common:3; Rare:99 | ||||
| chr2:188292764-188292855 | Common:1; Rare:23 | ||||
| chr2:188974297-188974564 | Rare:66; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189441133-189441433 | Common:1; Rare:73 | ||||
| chr2:189783965-189784085 | Common:3; Rare:42; Clinvar (benign):1 | ||||
| chr2:189784260-189784537 | Common:4; Rare:99; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:191014143-191014337 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677858-191678161 | Common:4; Rare:85 | ||||
| chr2:196362116-196362361 | Rare:41 | ||||
| chr2:197434973-197435186 | Rare:73 | ||||
| chr2:197499807-197500248 | Rare:165; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500263-197500430 | Common:1; Rare:69 |