| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53299589-53299767 | Common:3; Rare:89 | ||||
| chr12:53321240-53321414 | Common:1; Rare:63; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53380059-53380275 | Common:4; Rare:86 | ||||
| chr12:53441385-53441798 | Common:1; Rare:115 | ||||
| chr12:53499444-53499772 | Rare:68 | ||||
| chr12:53500153-53500248 | Rare:15 | ||||
| chr12:53500663-53500929 | Common:3; Rare:62 | ||||
| chr12:53501213-53501356 | Rare:35 | ||||
| chr12:53501509-53501596 | Rare:22 | ||||
| chr12:53625942-53626178 | Common:1; Rare:59 | ||||
| chr12:53626308-53626483 | Common:3; Rare:52 | ||||
| chr12:53676057-53676416 | Common:3; Rare:156 | ||||
| chr12:53727403-53727621 | Rare:48 | ||||
| chr12:54279688-54279863 | Rare:57 | ||||
| chr12:54281179-54281516 | Common:3; Rare:100 |