| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95858822-95859075 | Common:3; Rare:74 | ||||
| chr12:95943212-95943351 | Rare:22 | ||||
| chr12:95996260-95996523 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96013748-96014055 | Common:2; Rare:66 | ||||
| chr12:96035387-96035448 | Rare:18 | ||||
| chr12:96194245-96194638 | Common:6; Rare:125 | ||||
| chr12:96246825-96246961 | Common:1; Rare:36 | ||||
| chr12:96399993-96400324 | Common:1; Rare:98 | ||||
| chr12:96400527-96400645 | Common:1; Rare:52 | ||||
| chr12:96907190-96907290 | Rare:38 | ||||
| chr12:98515353-98516134 | Common:3; Rare:287; Clinvar:12; Clinvar (benign):10 | ||||
| chr12:98593469-98593776 | Common:2; Rare:100; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644703-98644873 | Common:3; Rare:53 | ||||
| chr12:98644986-98645313 | Common:2; Rare:97 | ||||
| chr12:100142824-100143220 | Common:5; Rare:124 |