| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95474006-95474211 | Common:2; Rare:98 | ||||
| chr12:95858822-95859037 | Common:2; Rare:58 | ||||
| chr12:96035555-96035758 | Common:2; Rare:43 | ||||
| chr12:96194224-96194535 | Common:5; Rare:108 | ||||
| chr12:96489452-96489610 | Common:2; Rare:40 | ||||
| chr12:96907139-96907290 | Common:1; Rare:52 | ||||
| chr12:98515431-98515807 | Rare:125; Clinvar:3 | ||||
| chr12:98515836-98516056 | Rare:81; Clinvar:5; Clinvar (benign):4 | ||||
| chr12:98593456-98593771 | Common:2; Rare:105; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644691-98644844 | Common:3; Rare:52 | ||||
| chr12:98644982-98645296 | Common:2; Rare:93 | ||||
| chr12:100267047-100267197 | Common:1; Rare:76 | ||||
| chr12:100573549-100573740 | Rare:66 | ||||
| chr12:101280026-101280143 | Common:1; Rare:35 | ||||
| chr12:101407668-101408035 | Common:3; Rare:89 |