| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2835005-2835056 | Rare:16 | ||||
| chr12:2877022-2877262 | Rare:71 | ||||
| chr12:2890706-2890938 | Common:1; Rare:92 | ||||
| chr12:3491313-3491434 | Rare:23 | ||||
| chr12:3873359-3873535 | Common:1; Rare:40 | ||||
| chr12:4273615-4273832 | Rare:61 | ||||
| chr12:4275455-4275631 | Common:2; Rare:26 | ||||
| chr12:4320957-4321258 | Common:5; Rare:113 | ||||
| chr12:4538429-4538914 | Common:2; Rare:108 | ||||
| chr12:4649045-4649158 | Common:1; Rare:48; Clinvar (benign):2 | ||||
| chr12:6375360-6375541 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6452070-6452119 | Common:1; Rare:11 | ||||
| chr12:6470633-6470757 | Common:1; Rare:48 | ||||
| chr12:6493234-6493386 | Common:6; Rare:42 | ||||
| chr12:6493768-6494132 | Common:2; Rare:109 |