| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4538436-4538932 | Common:3; Rare:113 | ||||
| chr12:4649010-4649178 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr12:4909694-4909916 | Common:3; Rare:42 | ||||
| chr12:6451780-6452120 | Common:4; Rare:62 | ||||
| chr12:6493240-6493386 | Common:5; Rare:41 | ||||
| chr12:6493746-6494138 | Common:2; Rare:116 | ||||
| chr12:6534284-6534578 | Common:5; Rare:122 | ||||
| chr12:6534616-6534860 | Common:3; Rare:99 | ||||
| chr12:6568260-6568354 | Rare:35 | ||||
| chr12:6663085-6663427 | Common:2; Rare:97 | ||||
| chr12:6723956-6724172 | Rare:57 | ||||
| chr12:6724193-6724296 | Rare:23 | ||||
| chr12:6752938-6753158 | Common:5; Rare:63 | ||||
| chr12:6851243-6851472 | Rare:54 | ||||
| chr12:6851921-6852174 | Rare:63 |