| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49357662-49357714 | Rare:16 | ||||
| chr3:50355520-50355820 | Common:1; Rare:55 | ||||
| chr3:52515429-52515596 | Rare:57 | ||||
| chr3:52595194-52595410 | Common:2; Rare:36 | ||||
| chr3:61560953-61561037 | Common:2; Rare:24 | ||||
| chr3:61564179-61564455 | Rare:69 | ||||
| chr3:64604072-64604253 | Common:2; Rare:60 | ||||
| chr3:64685003-64685348 | Rare:78 | ||||
| chr3:75435043-75435390 | Common:4; Rare:122 | ||||
| chr3:81761492-81761627 | Common:6; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:99789443-99789495 | Common:1; Rare:7 | ||||
| chr3:100754611-100754758 | Common:1; Rare:26 | ||||
| chr3:100775206-100775513 | Common:1; Rare:71 | ||||
| chr3:101576982-101577183 | Common:1; Rare:50 | ||||
| chr3:101676254-101676514 | Common:2; Rare:89 |