| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31326043-31326486 | Common:4; Rare:140 | ||||
| chr12:31589630-31590000 | Common:1; Rare:83 | ||||
| chr12:31591127-31591318 | Rare:69 | ||||
| chr12:31659083-31659425 | Common:2; Rare:84 | ||||
| chr12:31728792-31729365 | Common:3; Rare:161 | ||||
| chr12:31959258-31959494 | Common:2; Rare:77 | ||||
| chr12:31959616-31959866 | Common:2; Rare:84 | ||||
| chr12:32106507-32106962 | Common:6; Rare:122 | ||||
| chr12:32399259-32399659 | Common:7; Rare:133 | ||||
| chr12:32501907-32502264 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32502469-32502664 | Rare:28 | ||||
| chr12:32679057-32679443 | Common:2; Rare:143; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32679510-32679860 | Common:2; Rare:85 | ||||
| chr12:32755878-32756052 | Common:1; Rare:56 | ||||
| chr12:32896680-32897120 | Common:4; Rare:143; Clinvar:6; Clinvar (benign):8 |