| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:67269468-67269644 | Rare:47 | ||||
| chr12:68332288-68332615 | Common:1; Rare:100 | ||||
| chr12:68610660-68610992 | Common:1; Rare:149 | ||||
| chr12:69470294-69470429 | Common:2; Rare:49 | ||||
| chr12:75390912-75391105 | Common:1; Rare:59 | ||||
| chr12:76083921-76084126 | Rare:61 | ||||
| chr12:76348398-76348474 | Common:1; Rare:25; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:79934903-79935350 | Common:1; Rare:175 | ||||
| chr12:82358366-82358552 | Rare:78 | ||||
| chr12:82358736-82358887 | Common:3; Rare:79 | ||||
| chr12:88142075-88142373 | Rare:80; Clinvar:3 | ||||
| chr12:88580464-88580543 | Common:1; Rare:27 | ||||
| chr12:89352388-89352700 | Rare:84 | ||||
| chr12:89524748-89524869 | Common:1; Rare:22 | ||||
| chr12:92929218-92929484 | Common:1; Rare:82 |