| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120117116-120117348 | Common:3; Rare:71 | ||||
| chr12:120117499-120117511 | Rare:3 | ||||
| chr12:120117552-120117620 | Rare:11 | ||||
| chr12:120194455-120195150 | Common:3; Rare:191 | ||||
| chr12:120200709-120200844 | Rare:52 | ||||
| chr12:120200939-120201595 | Common:3; Rare:181 | ||||
| chr12:120201639-120201853 | Rare:45 | ||||
| chr12:120215634-120215896 | Rare:64 | ||||
| chr12:120224700-120224823 | Common:2; Rare:40 | ||||
| chr12:120225877-120226113 | Common:1; Rare:38 | ||||
| chr12:120248685-120248808 | Common:2; Rare:10 | ||||
| chr12:120265648-120265799 | Rare:82 | ||||
| chr12:120302031-120302374 | Common:2; Rare:64 | ||||
| chr12:120302575-120302606 | Rare:5 | ||||
| chr12:120437788-120438152 | Common:2; Rare:115; Clinvar (benign):1 |