| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31981627-31981808 | Common:1; Rare:47 | ||||
| chr3:32106378-32106670 | Common:4; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502795-32502938 | Rare:31 | ||||
| chr3:32570747-32570994 | Common:1; Rare:105 | ||||
| chr3:32685050-32685361 | Rare:96 | ||||
| chr3:33097104-33097239 | Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33718058-33718308 | Rare:92 | ||||
| chr3:33798520-33798639 | Common:2; Rare:34 | ||||
| chr3:36908511-36908543 | Rare:6 | ||||
| chr3:36993062-36993589 | Common:2; Rare:184; Clinvar:35; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
| chr3:36993663-36993833 | Rare:71; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:37243146-37243378 | Common:1; Rare:63 | ||||
| chr3:37994119-37994181 | Rare:21 | ||||
| chr3:37998977-37999147 | Common:1; Rare:62 | ||||
| chr3:38024518-38024664 | Common:1; Rare:57 |