| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32107305-32107518 | Common:1; Rare:75 | ||||
| chr12:32755884-32756028 | Common:1; Rare:45 | ||||
| chr12:38905491-38905733 | Common:3; Rare:68 | ||||
| chr12:38906282-38906534 | Common:2; Rare:51 | ||||
| chr12:38906713-38906799 | Common:1; Rare:22 | ||||
| chr12:40224969-40225116 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:42326065-42326215 | Common:1; Rare:47 | ||||
| chr12:43758743-43759009 | Common:2; Rare:75; Clinvar:2 | ||||
| chr12:43806269-43806397 | Common:2; Rare:42 | ||||
| chr12:45215982-45216174 | Common:1; Rare:63 | ||||
| chr12:45990392-45990959 | Common:2; Rare:182 | ||||
| chr12:46372674-46373065 | Common:1; Rare:148 | ||||
| chr12:47079527-47079629 | Common:1; Rare:20 | ||||
| chr12:47079697-47080052 | Common:4; Rare:86 | ||||
| chr12:47705970-47706093 | Rare:56 |