| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40453165-40453417 | Common:6; Rare:55 | ||||
| chr3:41201409-41201531 | Rare:24 | ||||
| chr3:41225468-41225844 | Rare:74; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:42632384-42632616 | Common:2; Rare:47 | ||||
| chr3:42654389-42654635 | Rare:72 | ||||
| chr3:44354592-44354779 | Rare:34 | ||||
| chr3:47164784-47165078 | Common:2; Rare:62 | ||||
| chr3:50252213-50252538 | Common:1; Rare:68 | ||||
| chr3:57013864-57013922 | Common:1; Rare:23 | ||||
| chr3:58059579-58059655 | Common:3; Rare:16 | ||||
| chr3:64561127-64561449 | Common:3; Rare:59 | ||||
| chr3:64561452-64561529 | Common:1; Rare:14 | ||||
| chr3:64561757-64561944 | Common:3; Rare:54 | ||||
| chr3:64572287-64572527 | Common:3; Rare:43 | ||||
| chr3:64684816-64685193 | Rare:74 |