| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:409910-411243 | Common:34; Rare:823 | ||||
| chr17:714697-715032 | Common:15; Rare:344; Clinvar (benign):2 | ||||
| chr17:731882-732282 | Rare:194 | ||||
| chr17:732240-732750 | Common:15; Rare:1081 | ||||
| chr17:733019-733448 | Common:12; Rare:272 | ||||
| chr17:751438-751838 | Rare:119 | ||||
| chr17:752108-753659 | Common:30; Rare:1117 | ||||
| chr17:781653-782102 | Common:5; Rare:199 | ||||
| chr17:782051-782651 | Common:17; Rare:1147 | ||||
| chr17:979670-980151 | Common:12; Rare:489 | ||||
| chr17:996590-996920 | Common:3; Rare:123 | ||||
| chr17:996862-997262 | Common:5; Rare:321 | ||||
| chr17:1115061-1115461 | Common:9; Rare:91 | ||||
| chr17:1179910-1180170 | Common:34; Rare:163 | ||||
| chr17:1364551-1365351 | Common:10; Rare:259 |