| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:70243321-70243773 | Common:4; Rare:141 | ||||
| chr12:71663763-71664067 | Common:1; Rare:86 | ||||
| chr12:71686014-71686548 | Common:4; Rare:149 | ||||
| chr12:71754737-71754900 | Common:2; Rare:37 | ||||
| chr12:71839668-71839806 | Common:1; Rare:56 | ||||
| chr12:74537753-74537887 | Common:1; Rare:54 | ||||
| chr12:75390870-75391119 | Common:1; Rare:75 | ||||
| chr12:75480594-75480933 | Rare:70 | ||||
| chr12:75511573-75511843 | Rare:81 | ||||
| chr12:76031389-76031883 | Common:1; Rare:156 | ||||
| chr12:76032148-76032315 | Rare:42 | ||||
| chr12:76053076-76053115 | Rare:6 | ||||
| chr12:76083928-76084068 | Rare:43 | ||||
| chr12:76348351-76348578 | Common:2; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559668-76559924 | Rare:92 |