| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:60135585-60135848 | Rare:75 | ||||
| chr17:60142192-60142342 | Common:2; Rare:26 | ||||
| chr17:60142938-60143364 | Common:6; Rare:166 | ||||
| chr17:60393218-60393322 | Common:1; Rare:14 | ||||
| chr17:60436021-60436168 | Rare:27 | ||||
| chr17:60601149-60601549 | Common:2; Rare:116; Clinvar (benign):1 | ||||
| chr17:60602078-60602198 | Rare:17 | ||||
| chr17:60743782-60744080 | Rare:50 | ||||
| chr17:61412435-61412626 | Common:3; Rare:72 | ||||
| chr17:61416854-61417001 | Common:1; Rare:30 | ||||
| chr17:61426009-61426409 | Common:5; Rare:138 | ||||
| chr17:61495175-61495477 | Rare:57 | ||||
| chr17:61495500-61495970 | Common:1; Rare:88 | ||||
| chr17:61496431-61497211 | Common:10; Rare:165 | ||||
| chr17:61556416-61556715 | Rare:46 |