| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36129724-36129996 | Common:2; Rare:102 | ||||
| chr18:36130240-36130318 | Rare:15 | ||||
| chr18:36187336-36187579 | Common:4; Rare:79 | ||||
| chr18:36187870-36187929 | Rare:20 | ||||
| chr18:36828745-36828920 | Rare:68 | ||||
| chr18:36828955-36829299 | Common:3; Rare:133 | ||||
| chr18:37254151-37254187 | Rare:10 | ||||
| chr18:41954990-41955284 | Common:2; Rare:103 | ||||
| chr18:41955427-41955492 | Common:1; Rare:27 | ||||
| chr18:44679797-44680178 | Common:1; Rare:49 | ||||
| chr18:45967228-45967592 | Common:1; Rare:129; Clinvar (pathogenic):1 | ||||
| chr18:46072233-46072300 | Common:1; Rare:19 | ||||
| chr18:46072357-46072395 | Common:1; Rare:8 | ||||
| chr18:46072433-46072483 | Rare:10 | ||||
| chr18:46088628-46088761 | Rare:35 |