| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71686194-71686420 | Common:1; Rare:65 | ||||
| chr12:71839572-71839802 | Common:2; Rare:81 | ||||
| chr12:74537717-74537889 | Common:1; Rare:67 | ||||
| chr12:75390873-75391109 | Common:1; Rare:70 | ||||
| chr12:75481554-75481881 | Common:2; Rare:69 | ||||
| chr12:76030875-76031111 | Rare:78 | ||||
| chr12:76031593-76031841 | Common:1; Rare:82 | ||||
| chr12:76083908-76084076 | Rare:50 | ||||
| chr12:76348351-76348525 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559764-76559890 | Rare:53 | ||||
| chr12:76764046-76764276 | Common:2; Rare:95 | ||||
| chr12:76879000-76879302 | Rare:86 | ||||
| chr12:78864569-78864842 | Common:2; Rare:57 | ||||
| chr12:79690493-79690639 | Rare:38 | ||||
| chr12:79690965-79691221 | Common:1; Rare:85 |