| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48105992-48106158 | Common:2; Rare:51 | ||||
| chr12:48106277-48106375 | Rare:29 | ||||
| chr12:48350877-48351094 | Common:5; Rare:81 | ||||
| chr12:48716672-48717046 | Common:4; Rare:114 | ||||
| chr12:48814747-48814862 | Rare:20 | ||||
| chr12:48815432-48815595 | Common:1; Rare:39 | ||||
| chr12:48852086-48852258 | Common:1; Rare:56 | ||||
| chr12:48939653-48940028 | Common:2; Rare:83 | ||||
| chr12:48957314-48957581 | Common:2; Rare:75 | ||||
| chr12:49018733-49018937 | Common:1; Rare:84 | ||||
| chr12:49069940-49070144 | Common:2; Rare:51 | ||||
| chr12:49110845-49111045 | Rare:48 | ||||
| chr12:49131302-49131617 | Common:2; Rare:124 | ||||
| chr12:49188488-49188607 | Common:2; Rare:17 | ||||
| chr12:49188981-49189298 | Rare:89; Clinvar:2; Clinvar (benign):2 |