| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44211296-44211358 | Rare:17 | ||||
| chr17:44221251-44221451 | Rare:56 | ||||
| chr17:44321447-44321708 | Common:1; Rare:107 | ||||
| chr17:44324771-44325003 | Common:2; Rare:83 | ||||
| chr17:44325342-44325471 | Common:3; Rare:28 | ||||
| chr17:44503366-44503722 | Rare:137 | ||||
| chr17:44899369-44899788 | Common:3; Rare:129; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:45051453-45051687 | Common:1; Rare:84 | ||||
| chr17:45060964-45061339 | Common:2; Rare:98 | ||||
| chr17:45132285-45132631 | Common:2; Rare:107 | ||||
| chr17:45148152-45148637 | Common:1; Rare:165 | ||||
| chr17:45161494-45161911 | Common:1; Rare:109 | ||||
| chr17:45425571-45425859 | Common:1; Rare:50 | ||||
| chr17:45431923-45432019 | Common:2; Rare:13 | ||||
| chr17:45490701-45490900 | Common:1; Rare:68 |