| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58433792-58433979 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58491747-58492150 | Common:3; Rare:103 | ||||
| chr3:59049968-59050159 | Rare:68 | ||||
| chr3:62318886-62319085 | Rare:84 | ||||
| chr3:63863773-63864170 | Common:8; Rare:130 | ||||
| chr3:63864424-63864573 | Common:2; Rare:53 | ||||
| chr3:63912381-63912710 | Common:2; Rare:138 | ||||
| chr3:64013720-64013781 | Rare:14 | ||||
| chr3:64018602-64019040 | Common:2; Rare:113 | ||||
| chr3:64023274-64023541 | Common:2; Rare:113 | ||||
| chr3:64687594-64687725 | Rare:34 | ||||
| chr3:64687987-64688188 | Common:1; Rare:58 | ||||
| chr3:66038636-66038934 | Common:3; Rare:97 | ||||
| chr3:67654485-67654786 | Common:2; Rare:120 | ||||
| chr3:69013574-69013803 | Common:1; Rare:67 |