| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48908300-48908407 | Common:1; Rare:25 | ||||
| chr17:48944754-48944918 | Common:2; Rare:59 | ||||
| chr17:49210205-49210432 | Common:2; Rare:33 | ||||
| chr17:49210508-49210719 | Rare:35 | ||||
| chr17:49362469-49362584 | Rare:30 | ||||
| chr17:49414833-49415143 | Common:2; Rare:76 | ||||
| chr17:49677936-49678331 | Rare:93 | ||||
| chr17:49788546-49788750 | Common:1; Rare:66 | ||||
| chr17:50055697-50055809 | Common:2; Rare:22 | ||||
| chr17:50055813-50056165 | Common:4; Rare:76 | ||||
| chr17:50056270-50056625 | Common:1; Rare:89 | ||||
| chr17:50188784-50189010 | Rare:61; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:50189174-50189683 | Rare:114; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:50345926-50346164 | Common:4; Rare:78 | ||||
| chr17:50373143-50373253 | Common:3; Rare:53 |