| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:132417405-132417565 | Common:2; Rare:57 | ||||
| chr3:132417880-132418020 | Rare:47 | ||||
| chr3:132418115-132418376 | Common:1; Rare:60 | ||||
| chr3:132626779-132627361 | Common:7; Rare:237 | ||||
| chr3:132659789-132659968 | Common:3; Rare:43 | ||||
| chr3:132660057-132660405 | Common:2; Rare:77 | ||||
| chr3:132660644-132661044 | Common:2; Rare:123 | ||||
| chr3:132721819-132722219 | Common:2; Rare:230; Clinvar:35; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr3:133038140-133038390 | Common:1; Rare:84 | ||||
| chr3:133124530-133124880 | Common:1; Rare:66 | ||||
| chr3:133573170-133573740 | Common:6; Rare:159 | ||||
| chr3:133573814-133573982 | Rare:45 | ||||
| chr3:133574166-133574839 | Common:12; Rare:385 | ||||
| chr3:133661849-133662041 | Rare:46 | ||||
| chr3:133805687-133805860 | Common:1; Rare:70 |