| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107760972-107761354 | Common:7; Rare:145 | ||||
| chr12:107761734-107761766 | Rare:5 | ||||
| chr12:108129535-108129784 | Common:1; Rare:55 | ||||
| chr12:108514962-108515356 | Common:1; Rare:122 | ||||
| chr12:108560969-108561268 | Common:2; Rare:112 | ||||
| chr12:108561387-108561592 | Common:2; Rare:39 | ||||
| chr12:108562032-108562132 | Common:2; Rare:10 | ||||
| chr12:108562303-108562667 | Common:11; Rare:136; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:108730405-108730588 | Common:1; Rare:51 | ||||
| chr12:108730591-108730684 | Rare:19 | ||||
| chr12:108730742-108730990 | Common:1; Rare:49 | ||||
| chr12:108731453-108731791 | Common:3; Rare:112 | ||||
| chr12:108731885-108732409 | Common:4; Rare:112 | ||||
| chr12:108857546-108857932 | Common:5; Rare:171 | ||||
| chr12:108857954-108857992 | Rare:8 |