| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3490748-3490962 | Rare:41 | ||||
| chr12:4273610-4274232 | Common:2; Rare:169; Clinvar (benign):1 | ||||
| chr12:4275601-4275704 | Common:1; Rare:23 | ||||
| chr12:4275741-4276224 | Rare:99 | ||||
| chr12:4321069-4321298 | Common:4; Rare:90 | ||||
| chr12:4538408-4538924 | Common:2; Rare:122 | ||||
| chr12:4648963-4649178 | Common:2; Rare:70; Clinvar (benign):2 | ||||
| chr12:6199992-6200486 | Common:4; Rare:143 | ||||
| chr12:6375370-6375552 | Common:2; Rare:39; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6384427-6384645 | Common:1; Rare:59 | ||||
| chr12:6388400-6388837 | Rare:112 | ||||
| chr12:6451785-6452159 | Common:4; Rare:70 | ||||
| chr12:6493060-6493394 | Common:7; Rare:97 | ||||
| chr12:6493788-6494140 | Common:2; Rare:106 | ||||
| chr12:6536476-6536707 | Rare:83 |