| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:70242855-70243030 | Common:1; Rare:61 | ||||
| chr12:71663019-71663188 | Rare:49 | ||||
| chr12:71663729-71664030 | Common:2; Rare:87 | ||||
| chr12:71664093-71664484 | Rare:108 | ||||
| chr12:72272353-72272535 | Rare:32 | ||||
| chr12:72272541-72272795 | Common:7; Rare:79 | ||||
| chr12:72273231-72273435 | Common:1; Rare:59 | ||||
| chr12:72273487-72273561 | Rare:27 | ||||
| chr12:74537717-74537876 | Common:1; Rare:62 | ||||
| chr12:75390873-75391089 | Common:1; Rare:57 | ||||
| chr12:75480549-75480909 | Rare:72 | ||||
| chr12:76031556-76031844 | Common:1; Rare:99 | ||||
| chr12:76084568-76084764 | Common:1; Rare:71 | ||||
| chr12:76348350-76348481 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559527-76559884 | Common:2; Rare:122 |