| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95003660-95003833 | Common:3; Rare:67; Clinvar (benign):3 | ||||
| chr12:95073485-95073647 | Common:1; Rare:64 | ||||
| chr12:95217384-95217774 | Common:4; Rare:110 | ||||
| chr12:95474055-95474224 | Common:2; Rare:84 | ||||
| chr12:95858822-95859075 | Common:3; Rare:74 | ||||
| chr12:96194220-96194554 | Common:5; Rare:113 | ||||
| chr12:96399369-96399476 | Common:1; Rare:32 | ||||
| chr12:96400559-96400689 | Rare:61 | ||||
| chr12:96489452-96489615 | Common:2; Rare:40 | ||||
| chr12:96907162-96907293 | Common:1; Rare:46 | ||||
| chr12:98515428-98515653 | Rare:77; Clinvar:1 | ||||
| chr12:98515844-98515876 | Rare:16; Clinvar (benign):1 | ||||
| chr12:98593474-98593776 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98645013-98645296 | Common:2; Rare:85 | ||||
| chr12:100142842-100143133 | Common:3; Rare:94 |