| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42998332-42998554 | Common:4; Rare:65 | ||||
| chr17:43017858-43018142 | Rare:84 | ||||
| chr17:43022342-43022685 | Rare:76 | ||||
| chr17:43125359-43125694 | Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170292-43170507 | Common:2; Rare:43 | ||||
| chr17:43170965-43171251 | Rare:93 | ||||
| chr17:43398821-43399002 | Common:1; Rare:52 | ||||
| chr17:43483663-43484052 | Rare:107 | ||||
| chr17:43778827-43779087 | Common:1; Rare:64 | ||||
| chr17:43833114-43833322 | Common:2; Rare:60 | ||||
| chr17:43847016-43847208 | Rare:46 | ||||
| chr17:43907507-43907678 | Rare:55 | ||||
| chr17:44070631-44070947 | Common:3; Rare:111; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44086812-44087029 | Common:2; Rare:58 | ||||
| chr17:44123580-44123844 | Common:3; Rare:77 |