| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49829016-49829048 | Common:1; Rare:5 | ||||
| chr12:49842651-49843274 | Common:4; Rare:181; Clinvar (benign):1 | ||||
| chr12:50017334-50017383 | Rare:4 | ||||
| chr12:50024892-50024921 | Rare:4 | ||||
| chr12:50025052-50025124 | Rare:14 | ||||
| chr12:50025301-50025802 | Common:2; Rare:131 | ||||
| chr12:50057180-50057461 | Common:1; Rare:50 | ||||
| chr12:50057539-50057738 | Rare:63 | ||||
| chr12:50085005-50085118 | Rare:23 | ||||
| chr12:50085120-50085456 | Common:1; Rare:91 | ||||
| chr12:50103897-50104045 | Rare:38 | ||||
| chr12:50111692-50111908 | Rare:46 | ||||
| chr12:50112020-50112289 | Common:2; Rare:59 | ||||
| chr12:50112454-50112548 | Rare:18 | ||||
| chr12:50112576-50112673 | Rare:26 |