| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49366280-49366598 | Common:3; Rare:74 | ||||
| chr12:49367205-49367541 | Common:1; Rare:94 | ||||
| chr12:49568086-49568444 | Common:2; Rare:87 | ||||
| chr12:49623276-49623571 | Common:1; Rare:85 | ||||
| chr12:49741219-49741607 | Rare:111 | ||||
| chr12:49750505-49750631 | Rare:19 | ||||
| chr12:49758245-49758476 | Common:4; Rare:74 | ||||
| chr12:49828387-49828600 | Common:1; Rare:79 | ||||
| chr12:49842916-49843201 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr12:50025407-50025712 | Common:2; Rare:84 | ||||
| chr12:50085030-50085397 | Common:1; Rare:96 | ||||
| chr12:50085543-50085697 | Rare:37 | ||||
| chr12:50088018-50088356 | Common:1; Rare:86 | ||||
| chr12:50112023-50112300 | Common:2; Rare:62 | ||||
| chr12:50167304-50167623 | Common:2; Rare:94 |