| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:25195467-25195579 | Common:2; Rare:21 | ||||
| chr12:25195806-25195857 | Rare:13 | ||||
| chr12:25250006-25250313 | Common:1; Rare:65 | ||||
| chr12:25250752-25251232 | Rare:143; Clinvar:5; Clinvar (benign):7 | ||||
| chr12:25251237-25251378 | Rare:41 | ||||
| chr12:25958434-25958944 | Common:4; Rare:186 | ||||
| chr12:25959035-25959212 | Common:2; Rare:51 | ||||
| chr12:25959293-25959387 | Common:1; Rare:22 | ||||
| chr12:26122101-26122445 | Common:3; Rare:110; Clinvar:1 | ||||
| chr12:26124998-26125206 | Common:1; Rare:48 | ||||
| chr12:26125409-26125724 | Common:2; Rare:47 | ||||
| chr12:26195360-26195613 | Common:4; Rare:57 | ||||
| chr12:26195834-26195989 | Rare:42 | ||||
| chr12:26196054-26196137 | Rare:19 | ||||
| chr12:26832412-26832549 | Common:1; Rare:27 |