| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95218004-95218404 | Common:7; Rare:142 | ||||
| chr12:95473823-95474219 | Common:5; Rare:234 | ||||
| chr12:95485890-95486201 | Common:2; Rare:94 | ||||
| chr12:95790036-95790457 | Common:6; Rare:183 | ||||
| chr12:95790610-95790726 | Common:2; Rare:60 | ||||
| chr12:95791080-95791410 | Rare:98 | ||||
| chr12:95858794-95859063 | Common:5; Rare:151 | ||||
| chr12:95942820-95943140 | Common:4; Rare:116 | ||||
| chr12:95943212-95943359 | Rare:49 | ||||
| chr12:95943410-95943840 | Common:2; Rare:165 | ||||
| chr12:95996170-95996590 | Common:6; Rare:100; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:96035555-96035744 | Common:2; Rare:39 | ||||
| chr12:96194245-96194563 | Common:5; Rare:135 | ||||
| chr12:96906987-96907517 | Common:3; Rare:217 | ||||
| chr12:98515431-98515726 | Rare:166; Clinvar:2 |