| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49707254-49707764 | Common:2; Rare:143 | ||||
| chr12:49741176-49741679 | Rare:143 | ||||
| chr12:49741722-49741903 | Common:2; Rare:43 | ||||
| chr12:49741926-49742265 | Common:1; Rare:130 | ||||
| chr12:49742297-49742381 | Rare:19 | ||||
| chr12:49750512-49750645 | Rare:20 | ||||
| chr12:49827732-49827953 | Common:2; Rare:57 | ||||
| chr12:49828366-49828769 | Common:2; Rare:119 | ||||
| chr12:49829011-49829048 | Common:1; Rare:6 | ||||
| chr12:49842614-49842693 | Rare:19 | ||||
| chr12:49842791-49843259 | Common:2; Rare:151; Clinvar (benign):1 | ||||
| chr12:49967106-49967240 | Common:1; Rare:28 | ||||
| chr12:50025318-50025790 | Common:2; Rare:124 | ||||
| chr12:50057362-50057492 | Rare:17 | ||||
| chr12:50057519-50057777 | Rare:76 |