| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47705970-47706093 | Rare:56 | ||||
| chr12:47758123-47758213 | Rare:12 | ||||
| chr12:47758716-47759027 | Common:2; Rare:55 | ||||
| chr12:47819857-47820123 | Common:2; Rare:63 | ||||
| chr12:47904992-47905118 | Common:1; Rare:35; Clinvar:1 | ||||
| chr12:48105988-48106197 | Common:2; Rare:68 | ||||
| chr12:48106277-48106385 | Rare:34 | ||||
| chr12:48141231-48141356 | Common:1; Rare:22; Clinvar (benign):1 | ||||
| chr12:48350787-48350963 | Rare:64 | ||||
| chr12:48815379-48815617 | Common:1; Rare:55 | ||||
| chr12:48852086-48852371 | Common:2; Rare:85 | ||||
| chr12:48939653-48940028 | Common:2; Rare:83 | ||||
| chr12:49018735-49018928 | Common:1; Rare:78 | ||||
| chr12:49110661-49110944 | Rare:60 | ||||
| chr12:49131298-49131617 | Common:2; Rare:125 |