| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49828411-49828544 | Rare:40 | ||||
| chr12:49843080-49843165 | Rare:36 | ||||
| chr12:50025444-50025747 | Common:2; Rare:82 | ||||
| chr12:50085258-50085364 | Common:1; Rare:28 | ||||
| chr12:50167269-50167603 | Common:3; Rare:99 | ||||
| chr12:50283500-50283629 | Rare:37 | ||||
| chr12:50400716-50400968 | Rare:76 | ||||
| chr12:50401309-50401443 | Common:1; Rare:32 | ||||
| chr12:50763913-50764113 | Common:1; Rare:59 | ||||
| chr12:51026316-51026515 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048187-51048351 | Common:1; Rare:66 | ||||
| chr12:51172769-51172870 | Common:1; Rare:23 | ||||
| chr12:51238648-51238885 | Common:8; Rare:103 | ||||
| chr12:51269832-51270141 | Common:2; Rare:122 | ||||
| chr12:51270282-51270422 | Common:3; Rare:39 |