| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40287589-40287937 | Rare:97 | ||||
| chr17:40318085-40318297 | Common:1; Rare:47 | ||||
| chr17:40417858-40418205 | Rare:108 | ||||
| chr17:41521713-41521951 | Common:1; Rare:37 | ||||
| chr17:41525446-41525738 | Common:2; Rare:61 | ||||
| chr17:41527826-41527969 | Rare:53 | ||||
| chr17:41527973-41528118 | Common:1; Rare:43; Clinvar:1 | ||||
| chr17:41528125-41528548 | Common:3; Rare:115; Clinvar:3 | ||||
| chr17:41583092-41583478 | Common:5; Rare:137; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr17:41586308-41586860 | Common:8; Rare:208; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr17:41586862-41587208 | Common:3; Rare:78 | ||||
| chr17:41612128-41612812 | Common:3; Rare:242; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:41612872-41613148 | Common:1; Rare:45 | ||||
| chr17:41624072-41624671 | Common:7; Rare:245; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:41624715-41625073 | Common:1; Rare:88 |