| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42017390-42017487 | Rare:42 | ||||
| chr17:42535950-42536312 | Common:3; Rare:103; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:42577671-42577838 | Rare:82 | ||||
| chr17:42609265-42609730 | Common:9; Rare:195; Clinvar (benign):2 | ||||
| chr17:42682439-42682577 | Rare:32 | ||||
| chr17:42798654-42798785 | Rare:43 | ||||
| chr17:42964430-42964534 | Rare:50 | ||||
| chr17:42980478-42980586 | Common:1; Rare:46 | ||||
| chr17:43125362-43125705 | Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170204-43170378 | Rare:41 | ||||
| chr17:43171004-43171239 | Rare:74 | ||||
| chr17:43211778-43211892 | Common:1; Rare:24 | ||||
| chr17:44123633-44123869 | Common:3; Rare:65 | ||||
| chr17:44186705-44187050 | Rare:106 | ||||
| chr17:44187163-44187318 | Common:1; Rare:41 |