| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48106272-48106391 | Rare:39 | ||||
| chr12:48119190-48119398 | Common:2; Rare:42; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48151367-48151613 | Common:1; Rare:43 | ||||
| chr12:48350781-48351123 | Common:6; Rare:124 | ||||
| chr12:48351243-48351333 | Common:1; Rare:17 | ||||
| chr12:48716834-48717122 | Common:3; Rare:83 | ||||
| chr12:48814672-48814862 | Rare:34 | ||||
| chr12:48815434-48815618 | Common:1; Rare:43 | ||||
| chr12:48852086-48852409 | Common:2; Rare:90 | ||||
| chr12:48865864-48865955 | Rare:23 | ||||
| chr12:48957309-48957581 | Common:2; Rare:76 | ||||
| chr12:49018736-49018947 | Common:1; Rare:88 | ||||
| chr12:49130778-49130941 | Common:3; Rare:64 | ||||
| chr12:49131296-49131621 | Common:2; Rare:126 | ||||
| chr12:49188482-49188636 | Common:2; Rare:21 |