| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441880-93442136 | Common:2; Rare:83 | ||||
| chr12:93571609-93571890 | Common:6; Rare:104 | ||||
| chr12:94459833-94460047 | Common:2; Rare:63 | ||||
| chr12:95217427-95217849 | Common:3; Rare:114 | ||||
| chr12:95474005-95474191 | Common:2; Rare:87 | ||||
| chr12:98515431-98515878 | Rare:161; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98593494-98593765 | Common:1; Rare:93; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644982-98645293 | Common:2; Rare:92 | ||||
| chr12:100267051-100267277 | Common:1; Rare:109 | ||||
| chr12:101407731-101408035 | Common:2; Rare:73 | ||||
| chr12:102120048-102120257 | Rare:84 | ||||
| chr12:103930066-103930549 | Common:8; Rare:164 | ||||
| chr12:103965664-103965941 | Common:2; Rare:73 | ||||
| chr12:104064435-104064548 | Rare:26 |