| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62584955-62585047 | Rare:14 | ||||
| chr12:62602408-62602868 | Common:3; Rare:159 | ||||
| chr12:62603491-62604175 | Common:2; Rare:180 | ||||
| chr12:62606792-62607114 | Common:3; Rare:56 | ||||
| chr12:62817179-62817389 | Common:2; Rare:42 | ||||
| chr12:63822379-63822679 | Common:1; Rare:50 | ||||
| chr12:63823965-63824080 | Common:2; Rare:17 | ||||
| chr12:63871567-63871623 | Rare:4 | ||||
| chr12:63916572-63916769 | Common:2; Rare:26 | ||||
| chr12:63918877-63918971 | Rare:14 | ||||
| chr12:63992824-63992876 | Rare:7 | ||||
| chr12:64086747-64087025 | Common:1; Rare:59 | ||||
| chr12:64314339-64314475 | Common:3; Rare:24 | ||||
| chr12:64442031-64442083 | Rare:16 | ||||
| chr12:64455614-64455958 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):2 |