| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40480690-40480718 | Rare:7 | ||||
| chr17:40480995-40481314 | Rare:50 | ||||
| chr17:40501504-40501756 | Common:1; Rare:51 | ||||
| chr17:40560338-40560559 | Common:2; Rare:51 | ||||
| chr17:40647353-40647485 | Rare:37 | ||||
| chr17:40647734-40647872 | Rare:36 | ||||
| chr17:40648006-40648368 | Common:1; Rare:88 | ||||
| chr17:40648389-40648732 | Rare:59 | ||||
| chr17:40818771-40819211 | Common:13; Rare:282; Clinvar (benign):2 | ||||
| chr17:40819548-40819673 | Rare:36; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:41521749-41521960 | Common:1; Rare:28 | ||||
| chr17:41586866-41587103 | Common:1; Rare:53 | ||||
| chr17:41612727-41612902 | Rare:30 | ||||
| chr17:41624366-41624428 | Rare:26 | ||||
| chr17:41624439-41625049 | Common:8; Rare:179; Clinvar (benign):1 |