| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43211758-43211921 | Common:1; Rare:36 | ||||
| chr17:43398916-43399009 | Rare:23 | ||||
| chr17:43546299-43546615 | Common:2; Rare:73 | ||||
| chr17:43833104-43833318 | Common:2; Rare:61 | ||||
| chr17:43900557-43900799 | Rare:85 | ||||
| chr17:44004473-44004623 | Rare:35 | ||||
| chr17:44066040-44066348 | Common:1; Rare:78 | ||||
| chr17:44070327-44070392 | Rare:7 | ||||
| chr17:44070612-44071007 | Common:3; Rare:136; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123588-44123840 | Common:3; Rare:72 | ||||
| chr17:44141775-44142062 | Common:1; Rare:70 | ||||
| chr17:44186620-44187037 | Common:1; Rare:145 | ||||
| chr17:44187152-44187279 | Rare:32 | ||||
| chr17:44187449-44187516 | Rare:15 | ||||
| chr17:44199329-44199503 | Common:1; Rare:53 |