| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42566974-42567161 | Common:3; Rare:63 | ||||
| chr17:42577578-42577844 | Rare:126 | ||||
| chr17:42609233-42609779 | Common:9; Rare:223; Clinvar (benign):2 | ||||
| chr17:42659357-42659428 | Rare:18 | ||||
| chr17:42676944-42677331 | Common:1; Rare:100 | ||||
| chr17:42682417-42682586 | Rare:40 | ||||
| chr17:42745023-42745151 | Common:3; Rare:46 | ||||
| chr17:42773127-42773506 | Rare:84 | ||||
| chr17:42798463-42798792 | Rare:114; Clinvar (pathogenic):1 | ||||
| chr17:42798795-42798863 | Rare:19 | ||||
| chr17:42833329-42833685 | Common:2; Rare:114 | ||||
| chr17:42834348-42834877 | Common:2; Rare:127 | ||||
| chr17:42964417-42964567 | Common:1; Rare:64 | ||||
| chr17:42980380-42980586 | Common:1; Rare:64 | ||||
| chr17:42998237-42998553 | Common:4; Rare:88 |