| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53252009-53252208 | Common:3; Rare:78 | ||||
| chr12:53295442-53295591 | Common:1; Rare:54 | ||||
| chr12:53321232-53321358 | Rare:36 | ||||
| chr12:53501192-53501352 | Rare:38 | ||||
| chr12:53626333-53626511 | Common:3; Rare:47 | ||||
| chr12:53727425-53727768 | Rare:79 | ||||
| chr12:53984996-53985267 | Common:2; Rare:71 | ||||
| chr12:53999960-54000126 | Common:4; Rare:44 | ||||
| chr12:54259526-54259724 | Rare:38 | ||||
| chr12:54391300-54391411 | Rare:24 | ||||
| chr12:54419213-54419421 | Common:1; Rare:58 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:55712080-55712354 | Common:7; Rare:71; Clinvar (benign):1 | ||||
| chr12:55716003-55716195 | Common:1; Rare:91 | ||||
| chr12:55716424-55716602 | Common:3; Rare:46 |