| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44685567-44685716 | Common:1; Rare:47 | ||||
| chr3:44899980-44900560 | Common:4; Rare:102 | ||||
| chr3:45167657-45167782 | Common:1; Rare:26 | ||||
| chr3:45225059-45225363 | Common:2; Rare:60 | ||||
| chr3:46629795-46629975 | Common:2; Rare:27 | ||||
| chr3:47009260-47009590 | Common:5; Rare:126; Clinvar:5; Clinvar (benign):4 | ||||
| chr3:47164710-47165050 | Common:3; Rare:72 | ||||
| chr3:47522179-47522379 | Common:1; Rare:37 | ||||
| chr3:47571369-47571616 | Common:1; Rare:54 | ||||
| chr3:47573430-47573800 | Common:1; Rare:60 | ||||
| chr3:47889785-47890348 | Common:4; Rare:166 | ||||
| chr3:48023397-48023797 | Rare:100 | ||||
| chr3:48039272-48039416 | Rare:28 | ||||
| chr3:48039927-48040095 | Rare:26 | ||||
| chr3:48040169-48040569 | Common:3; Rare:106 |