| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57431412-57431448 | Rare:4 | ||||
| chr12:57454554-57454738 | Rare:43 | ||||
| chr12:57454941-57455166 | Rare:45 | ||||
| chr12:57455749-57455998 | Common:1; Rare:51 | ||||
| chr12:57487795-57488152 | Common:1; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:57515595-57515865 | Common:1; Rare:43 | ||||
| chr12:57520414-57520999 | Common:4; Rare:162 | ||||
| chr12:57522210-57522394 | Common:1; Rare:38 | ||||
| chr12:57522416-57522740 | Common:1; Rare:94 | ||||
| chr12:57522803-57522967 | Common:1; Rare:46 | ||||
| chr12:57523151-57523297 | Rare:32 | ||||
| chr12:57523536-57523556 | Rare:4 | ||||
| chr12:57546309-57546637 | Rare:64 | ||||
| chr12:57546776-57546829 | Common:1; Rare:8 | ||||
| chr12:57547086-57547427 | Common:1; Rare:71 |