| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96400541-96400651 | Rare:51 | ||||
| chr12:96489443-96489630 | Common:2; Rare:49 | ||||
| chr12:96907162-96907290 | Common:1; Rare:45 | ||||
| chr12:98515431-98515784 | Rare:116; Clinvar:2 | ||||
| chr12:98593462-98593919 | Common:2; Rare:140; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644737-98645299 | Common:5; Rare:163 | ||||
| chr12:98894708-98895021 | Common:3; Rare:129 | ||||
| chr12:99154447-99154895 | Common:1; Rare:99 | ||||
| chr12:99154907-99155002 | Rare:21 | ||||
| chr12:99984227-99984383 | Rare:37 | ||||
| chr12:99984701-99985003 | Common:2; Rare:99 | ||||
| chr12:100200707-100200863 | Rare:50 | ||||
| chr12:100267047-100267383 | Common:1; Rare:141 | ||||
| chr12:100573607-100573762 | Rare:49 | ||||
| chr12:100794805-100794911 | Rare:20 |