| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63697921-63698199 | Common:2; Rare:55 | ||||
| chr17:63701921-63702156 | Common:3; Rare:93 | ||||
| chr17:63740962-63740982 | Rare:3 | ||||
| chr17:63742804-63742968 | Common:2; Rare:26 | ||||
| chr17:63839320-63839475 | Rare:20 | ||||
| chr17:63841596-63841797 | Common:1; Rare:40 | ||||
| chr17:63843581-63843787 | Common:1; Rare:20 | ||||
| chr17:63922674-63922717 | Rare:9 | ||||
| chr17:63927512-63927692 | Rare:28 | ||||
| chr17:63931296-63931548 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr17:63945734-63946065 | Common:2; Rare:57 | ||||
| chr17:63946420-63946503 | Common:6; Rare:34 | ||||
| chr17:63954413-63954590 | Rare:30 | ||||
| chr17:64016588-64016662 | Rare:7 | ||||
| chr17:64018524-64018556 | Rare:7 |