| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57692937-57693154 | Common:1; Rare:69 | ||||
| chr3:57889883-57890122 | Rare:52; Clinvar (benign):2 | ||||
| chr3:58008772-58008849 | Rare:14; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:58332665-58333039 | Common:10; Rare:88 | ||||
| chr3:58433799-58433921 | Rare:47; Clinvar (benign):3 | ||||
| chr3:59050066-59050108 | Rare:10 | ||||
| chr3:61251341-61251607 | Common:4; Rare:62 | ||||
| chr3:61561412-61561657 | Common:2; Rare:87 | ||||
| chr3:62318927-62319073 | Rare:57 | ||||
| chr3:63863743-63864167 | Common:8; Rare:140 | ||||
| chr3:63911996-63912116 | Rare:40 | ||||
| chr3:64225274-64225609 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:64687546-64687732 | Rare:46 | ||||
| chr3:64687982-64688197 | Common:1; Rare:60 | ||||
| chr3:64688270-64688385 | Rare:23 |