| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96035527-96035789 | Common:2; Rare:58 | ||||
| chr12:96194247-96194612 | Common:5; Rare:117 | ||||
| chr12:96400053-96400305 | Common:1; Rare:67 | ||||
| chr12:96400527-96400651 | Common:1; Rare:56 | ||||
| chr12:96489497-96489726 | Common:2; Rare:69 | ||||
| chr12:96907180-96907482 | Common:1; Rare:95 | ||||
| chr12:98515471-98515993 | Rare:177; Clinvar:9; Clinvar (benign):3 | ||||
| chr12:98516131-98516424 | Rare:100 | ||||
| chr12:98593474-98593876 | Common:2; Rare:126; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644711-98645327 | Common:7; Rare:178 | ||||
| chr12:98745849-98745950 | Rare:33 | ||||
| chr12:99079941-99080103 | Common:1; Rare:28 | ||||
| chr12:99647594-99647768 | Rare:41 | ||||
| chr12:99706632-99706749 | Common:1; Rare:22 | ||||
| chr12:99984703-99985056 | Common:3; Rare:106 |