| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:68808472-68808485 | Rare:3 | ||||
| chr12:68933153-68933343 | Rare:60 | ||||
| chr12:69348262-69348465 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr12:69470280-69470451 | Common:4; Rare:70 | ||||
| chr12:71663776-71664030 | Common:1; Rare:77 | ||||
| chr12:71686026-71686113 | Common:1; Rare:23 | ||||
| chr12:71686205-71686427 | Common:2; Rare:67 | ||||
| chr12:71754577-71754873 | Common:3; Rare:65 | ||||
| chr12:71839593-71839802 | Common:1; Rare:79 | ||||
| chr12:74537769-74537868 | Common:1; Rare:41 | ||||
| chr12:75390891-75391109 | Common:1; Rare:69 | ||||
| chr12:76031593-76031817 | Common:1; Rare:80 | ||||
| chr12:76559690-76559882 | Rare:75 | ||||
| chr12:76764040-76764567 | Common:2; Rare:201 | ||||
| chr12:76878948-76879212 | Rare:92 |