| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48240934-48241129 | Common:1; Rare:54 | ||||
| chr3:48301340-48301666 | Common:4; Rare:103 | ||||
| chr3:48440048-48440324 | Common:1; Rare:108 | ||||
| chr3:48473015-48473242 | Common:1; Rare:50 | ||||
| chr3:48556762-48557054 | Common:1; Rare:73 | ||||
| chr3:48662893-48662996 | Rare:18 | ||||
| chr3:48918783-48918900 | Common:2; Rare:68 | ||||
| chr3:49007160-49007424 | Common:2; Rare:107 | ||||
| chr3:49022009-49022192 | Rare:63; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49104734-49104934 | Rare:79; Clinvar (benign):3 | ||||
| chr3:49120773-49121018 | Rare:69 | ||||
| chr3:49133003-49133107 | Rare:22 | ||||
| chr3:49340020-49340127 | Common:2; Rare:47 | ||||
| chr3:49358281-49358414 | Common:2; Rare:78 | ||||
| chr3:49411909-49412210 | Common:1; Rare:106 |