| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:33439730-33440220 | Common:4; Rare:141 | ||||
| chr12:34022110-34022570 | Common:3; Rare:115 | ||||
| chr12:38316380-38316870 | Common:10; Rare:115 | ||||
| chr12:38905445-38905862 | Common:10; Rare:185 | ||||
| chr12:38906600-38906950 | Common:2; Rare:68 | ||||
| chr12:39442389-39442539 | Rare:56 | ||||
| chr12:39443107-39443273 | Common:1; Rare:44; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:39443556-39443825 | Rare:61 | ||||
| chr12:39619789-39620115 | Common:2; Rare:52 | ||||
| chr12:40106013-40106237 | Common:1; Rare:91 | ||||
| chr12:40224310-40224740 | Common:1; Rare:105 | ||||
| chr12:42144618-42145030 | Common:8; Rare:172 | ||||
| chr12:42237310-42237860 | Common:1; Rare:152 | ||||
| chr12:42238140-42238590 | Common:5; Rare:140 | ||||
| chr12:42326006-42326223 | Common:1; Rare:70 |