| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49366697-49367048 | Common:2; Rare:92 | ||||
| chr12:49367084-49367753 | Common:4; Rare:163 | ||||
| chr12:49567787-49567935 | Rare:42 | ||||
| chr12:49568035-49568375 | Common:2; Rare:81 | ||||
| chr12:49568591-49568725 | Common:1; Rare:26 | ||||
| chr12:49623199-49623580 | Common:3; Rare:108 | ||||
| chr12:49706912-49707123 | Rare:63 | ||||
| chr12:49707226-49707468 | Common:2; Rare:68 | ||||
| chr12:49741216-49741634 | Rare:121 | ||||
| chr12:49741751-49741892 | Common:2; Rare:33 | ||||
| chr12:49742043-49742212 | Rare:75 | ||||
| chr12:49750512-49750616 | Rare:15 | ||||
| chr12:49828361-49828720 | Common:1; Rare:114 | ||||
| chr12:49842614-49842676 | Rare:16 | ||||
| chr12:49842682-49843257 | Common:4; Rare:168; Clinvar (benign):1 |