| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121579323-121579471 | Rare:32 | ||||
| chr12:121580029-121580554 | Rare:269 | ||||
| chr12:121580938-121581120 | Rare:68 | ||||
| chr12:121626220-121626706 | Common:6; Rare:485 | ||||
| chr12:121626707-121626946 | Common:11; Rare:295; Clinvar:13; Clinvar (benign):5 | ||||
| chr12:121627213-121627555 | Common:2; Rare:78 | ||||
| chr12:121672450-121672810 | Common:16; Rare:210 | ||||
| chr12:121712583-121712954 | Common:15; Rare:352 | ||||
| chr12:121793402-121794205 | Common:12; Rare:379 | ||||
| chr12:121794250-121794510 | Common:2; Rare:126 | ||||
| chr12:121799611-121800412 | Common:14; Rare:420 | ||||
| chr12:121800447-121800847 | Common:4; Rare:246 | ||||
| chr12:121800887-121801161 | Common:6; Rare:152 | ||||
| chr12:121802890-121803498 | Common:3; Rare:410 | ||||
| chr12:121803801-121804114 | Rare:256 |