| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96399321-96399955 | Common:2; Rare:188 | ||||
| chr12:96399993-96400790 | Common:3; Rare:266 | ||||
| chr12:96906986-96907382 | Common:3; Rare:133 | ||||
| chr12:98515256-98515742 | Common:1; Rare:162; Clinvar:1 | ||||
| chr12:98516125-98516581 | Common:4; Rare:151; Clinvar:1 | ||||
| chr12:98593374-98593810 | Common:2; Rare:143; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644374-98644469 | Rare:24 | ||||
| chr12:98644691-98644898 | Common:3; Rare:64 | ||||
| chr12:98644945-98645375 | Common:2; Rare:129 | ||||
| chr12:98645779-98645818 | Rare:13 | ||||
| chr12:100142349-100142504 | Rare:35 | ||||
| chr12:100142762-100143098 | Common:3; Rare:128 | ||||
| chr12:100199699-100200150 | Common:3; Rare:104 | ||||
| chr12:100200688-100200902 | Common:2; Rare:68 | ||||
| chr12:100266725-100266873 | Rare:35 |