| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96035531-96035777 | Common:2; Rare:53 | ||||
| chr12:96400559-96400682 | Rare:57 | ||||
| chr12:96907162-96907295 | Common:1; Rare:48 | ||||
| chr12:98515455-98515767 | Rare:99; Clinvar:2 | ||||
| chr12:98515833-98515870 | Rare:19; Clinvar (benign):1 | ||||
| chr12:98644974-98645307 | Common:2; Rare:99 | ||||
| chr12:100142850-100143016 | Common:2; Rare:59 | ||||
| chr12:100200707-100200834 | Rare:39 | ||||
| chr12:100267047-100267235 | Common:1; Rare:99 | ||||
| chr12:101209894-101209946 | Common:1; Rare:16 | ||||
| chr12:101407690-101408068 | Common:3; Rare:91 | ||||
| chr12:101616982-101617236 | Common:1; Rare:59 | ||||
| chr12:102120043-102120229 | Rare:73 | ||||
| chr12:103930077-103930571 | Common:8; Rare:166 | ||||
| chr12:103965705-103965941 | Common:2; Rare:55 |