| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95003593-95003830 | Common:3; Rare:99; Clinvar (benign):6 | ||||
| chr12:95073443-95073729 | Common:1; Rare:94 | ||||
| chr12:95217364-95217840 | Common:5; Rare:130 | ||||
| chr12:95473664-95474011 | Common:2; Rare:81 | ||||
| chr12:95474043-95474330 | Common:2; Rare:119 | ||||
| chr12:95943206-95943509 | Common:3; Rare:67 | ||||
| chr12:95995874-95996099 | Common:2; Rare:45; Clinvar:2 | ||||
| chr12:95996230-95996589 | Common:4; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96400556-96400690 | Rare:63 | ||||
| chr12:96907190-96907293 | Rare:39 | ||||
| chr12:98515428-98515814 | Rare:130; Clinvar:4 | ||||
| chr12:98593471-98593765 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644731-98644843 | Common:1; Rare:36 | ||||
| chr12:98644974-98645293 | Common:2; Rare:95 | ||||
| chr12:100142833-100143069 | Common:3; Rare:88 |