| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49007780-49008062 | Common:2; Rare:78 | ||||
| chr3:49017756-49017852 | Rare:36 | ||||
| chr3:49018368-49018737 | Common:2; Rare:131 | ||||
| chr3:49020276-49020495 | Common:1; Rare:35 | ||||
| chr3:49020498-49020597 | Rare:25 | ||||
| chr3:49021283-49021769 | Common:2; Rare:121; Clinvar:1 | ||||
| chr3:49021844-49022328 | Rare:154; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:49029318-49029626 | Common:2; Rare:200 | ||||
| chr3:49093444-49093684 | Common:1; Rare:84 | ||||
| chr3:49093984-49094221 | Rare:56 | ||||
| chr3:49094239-49094458 | Common:1; Rare:52 | ||||
| chr3:49104439-49104622 | Rare:68; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:49104668-49104994 | Common:1; Rare:127; Clinvar:2; Clinvar (benign):6 | ||||
| chr3:49120685-49121070 | Rare:110 | ||||
| chr3:49166270-49166490 | Common:1; Rare:55 |