| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58433793-58433927 | Rare:54; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:61251370-61251593 | Common:4; Rare:55 | ||||
| chr3:61561484-61561656 | Common:2; Rare:52 | ||||
| chr3:62318890-62319055 | Rare:69 | ||||
| chr3:63863773-63864171 | Common:8; Rare:130 | ||||
| chr3:63864446-63864555 | Common:2; Rare:41 | ||||
| chr3:63911974-63912112 | Rare:42 | ||||
| chr3:67654581-67654770 | Common:2; Rare:70 | ||||
| chr3:69013200-69013348 | Rare:43 | ||||
| chr3:69013579-69013830 | Common:1; Rare:76 | ||||
| chr3:69200469-69200658 | Common:2; Rare:31 | ||||
| chr3:70977641-70977874 | Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:71581851-71582184 | Common:1; Rare:76 | ||||
| chr3:71754758-71754860 | Rare:28 | ||||
| chr3:79018781-79019061 | Common:1; Rare:83 |