| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:19150902-19151180 | Common:1; Rare:62 | ||||
| chr12:19164749-19164950 | Rare:39 | ||||
| chr12:19198365-19198679 | Common:3; Rare:50 | ||||
| chr12:19213301-19213564 | Common:2; Rare:35 | ||||
| chr12:19213638-19213897 | Rare:42 | ||||
| chr12:19242554-19242769 | Common:1; Rare:41 | ||||
| chr12:19251690-19251732 | Rare:5 | ||||
| chr12:19269344-19269592 | Common:4; Rare:44 | ||||
| chr12:19297678-19297725 | Rare:6 | ||||
| chr12:19307571-19307739 | Rare:37 | ||||
| chr12:19316395-19316440 | Common:3; Rare:13 | ||||
| chr12:19347709-19347869 | Rare:25 | ||||
| chr12:19355370-19355377 | |||||
| chr12:19411896-19412118 | Rare:46 | ||||
| chr12:19512822-19512988 | Rare:39 |