| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48918692-48918934 | Common:2; Rare:125 | ||||
| chr3:48968322-48968642 | Rare:73 | ||||
| chr3:49007181-49007464 | Common:2; Rare:114 | ||||
| chr3:49014166-49014496 | Common:1; Rare:118 | ||||
| chr3:49018552-49018625 | Rare:26 | ||||
| chr3:49021498-49021721 | Rare:55; Clinvar:1 | ||||
| chr3:49022035-49022141 | Rare:35 | ||||
| chr3:49028290-49028364 | Rare:26 | ||||
| chr3:49029319-49029564 | Common:2; Rare:168 | ||||
| chr3:49093991-49094281 | Rare:71 | ||||
| chr3:49104416-49104891 | Common:1; Rare:185; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr3:49120758-49121005 | Rare:73 | ||||
| chr3:49132979-49133148 | Rare:37; Clinvar:1 | ||||
| chr3:49166289-49166442 | Common:1; Rare:40 | ||||
| chr3:49339968-49340201 | Common:2; Rare:96 |