| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51270339-51270367 | Common:1; Rare:7 | ||||
| chr12:51270371-51270540 | Common:2; Rare:42 | ||||
| chr12:51391402-51391472 | Rare:16 | ||||
| chr12:51391603-51391779 | Common:2; Rare:56 | ||||
| chr12:51424673-51424838 | Common:1; Rare:40 | ||||
| chr12:51912179-51912400 | Common:1; Rare:43 | ||||
| chr12:52006684-52006977 | Rare:65 | ||||
| chr12:52051115-52051572 | Common:1; Rare:148 | ||||
| chr12:52055857-52056149 | Common:3; Rare:89 | ||||
| chr12:52249123-52249335 | Rare:45 | ||||
| chr12:52902162-52902290 | Rare:21 | ||||
| chr12:52904632-52905348 | Common:7; Rare:207; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:52949768-52950033 | Rare:59 | ||||
| chr12:52951488-52951856 | Rare:100; Clinvar:5 | ||||
| chr12:53006238-53006495 | Common:2; Rare:97 |