| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95548663-95548914 | Common:6; Rare:71 | ||||
| chr12:95551229-95551761 | Common:5; Rare:107 | ||||
| chr12:95858804-95859073 | Common:3; Rare:81 | ||||
| chr12:95942909-95943064 | Common:1; Rare:35 | ||||
| chr12:96035365-96035414 | Rare:15 | ||||
| chr12:96035460-96035801 | Common:2; Rare:85 | ||||
| chr12:96194232-96194484 | Common:5; Rare:91 | ||||
| chr12:96907195-96907544 | Common:1; Rare:106 | ||||
| chr12:98515430-98515697 | Rare:88; Clinvar:1 | ||||
| chr12:98516152-98516296 | Rare:56 | ||||
| chr12:98516488-98516589 | Common:1; Rare:32 | ||||
| chr12:98545034-98545109 | Rare:20 | ||||
| chr12:98593395-98593790 | Common:2; Rare:135; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644680-98644843 | Common:3; Rare:56 | ||||
| chr12:98644916-98645298 | Common:4; Rare:111 |