| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49741193-49741663 | Rare:133 | ||||
| chr12:49741738-49742360 | Common:3; Rare:207 | ||||
| chr12:49750438-49750778 | Rare:46 | ||||
| chr12:49751072-49751118 | Rare:11 | ||||
| chr12:49828195-49828751 | Common:2; Rare:159 | ||||
| chr12:49828763-49828834 | Common:1; Rare:5 | ||||
| chr12:49829011-49829048 | Common:1; Rare:6 | ||||
| chr12:49842588-49842992 | Common:2; Rare:96 | ||||
| chr12:49842999-49843259 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:50017017-50017370 | Common:1; Rare:50 | ||||
| chr12:50025086-50025125 | Rare:7 | ||||
| chr12:50025321-50025352 | Rare:4 | ||||
| chr12:50025356-50025786 | Common:2; Rare:118 | ||||
| chr12:50057381-50057461 | Rare:9 | ||||
| chr12:50057519-50057766 | Rare:75 |