| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89351378-89351525 | Common:1; Rare:35 | ||||
| chr12:89352393-89352597 | Rare:57 | ||||
| chr12:89524748-89524904 | Common:2; Rare:28 | ||||
| chr12:89525882-89526127 | Common:1; Rare:93 | ||||
| chr12:89708809-89709003 | Rare:80 | ||||
| chr12:92145836-92146224 | Common:2; Rare:120 | ||||
| chr12:93441895-93442186 | Common:2; Rare:92 | ||||
| chr12:94459812-94460009 | Common:3; Rare:52 | ||||
| chr12:95003644-95003831 | Common:3; Rare:71; Clinvar (benign):3 | ||||
| chr12:95217455-95217843 | Common:3; Rare:104 | ||||
| chr12:95474101-95474314 | Common:2; Rare:99 | ||||
| chr12:96035533-96035783 | Common:2; Rare:55 | ||||
| chr12:96907135-96907274 | Common:1; Rare:47 | ||||
| chr12:98515392-98515682 | Common:1; Rare:101; Clinvar:1 | ||||
| chr12:98593493-98593765 | Common:1; Rare:93; Clinvar:4; Clinvar (benign):4 |