| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53097780-53098035 | Rare:69 | ||||
| chr12:53180451-53180730 | Common:2; Rare:107 | ||||
| chr12:53181313-53181491 | Rare:48 | ||||
| chr12:53232174-53232385 | Common:2; Rare:46 | ||||
| chr12:53252016-53252212 | Common:3; Rare:77 | ||||
| chr12:53499436-53499772 | Rare:70 | ||||
| chr12:53500215-53500290 | Rare:7 | ||||
| chr12:53500663-53500929 | Common:3; Rare:62 | ||||
| chr12:53501213-53501373 | Rare:39 | ||||
| chr12:53727419-53727704 | Rare:65 | ||||
| chr12:53999958-54000126 | Common:4; Rare:45 | ||||
| chr12:54028341-54028467 | Common:1; Rare:30 | ||||
| chr12:54259516-54259734 | Rare:40 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:55720168-55720398 | Common:3; Rare:28; Clinvar (benign):1 |