| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57751765-57751964 | Rare:89 | ||||
| chr12:57752237-57752739 | Common:3; Rare:556; Clinvar:4 | ||||
| chr12:57754086-57755098 | Common:11; Rare:419 | ||||
| chr12:57755860-57756755 | Common:6; Rare:423 | ||||
| chr12:57766363-57767078 | Common:2; Rare:240; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:57771128-57771528 | Common:2; Rare:126 | ||||
| chr12:57771614-57773113 | Common:31; Rare:1490 | ||||
| chr12:57782492-57782892 | Common:7; Rare:280; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr12:57845435-57846319 | Common:19; Rare:625 | ||||
| chr12:57846270-57847316 | Common:29; Rare:1382 | ||||
| chr12:57940737-57942042 | Common:31; Rare:960 | ||||
| chr12:62257977-62258837 | Common:1; Rare:187 | ||||
| chr12:62258828-62260480 | Common:11; Rare:1603 | ||||
| chr12:62260545-62260658 | Rare:19 | ||||
| chr12:62260745-62261420 | Common:1; Rare:555 |