| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56640884-56640977 | Common:1; Rare:10 | ||||
| chr12:56672835-56673062 | Rare:55 | ||||
| chr12:57068464-57068476 | Rare:2 | ||||
| chr12:57069417-57069436 | Rare:4 | ||||
| chr12:57420900-57421151 | Rare:40 | ||||
| chr12:57490337-57490576 | Rare:56; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:57518496-57518569 | Rare:12 | ||||
| chr12:57519179-57519234 | Rare:17 | ||||
| chr12:57519270-57519278 | |||||
| chr12:57519369-57519541 | Rare:33 | ||||
| chr12:57537079-57537352 | Rare:42 | ||||
| chr12:57653372-57653475 | Common:1; Rare:22 | ||||
| chr12:57688445-57688640 | Rare:25 | ||||
| chr12:57831082-57831099 | Rare:1 | ||||
| chr12:57836820-57837097 | Common:2; Rare:47 |