| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123671008-123671140 | Common:1; Rare:28 | ||||
| chr12:123972540-123972656 | Common:3; Rare:35 | ||||
| chr12:124786716-124786789 | Rare:19 | ||||
| chr12:124917618-124917780 | Rare:43 | ||||
| chr12:130716260-130716547 | Rare:43 | ||||
| chr12:130871755-130872126 | Common:4; Rare:148 | ||||
| chr12:131710779-131711113 | Rare:92 | ||||
| chr12:132275376-132275423 | Common:2; Rare:11 | ||||
| chr12:132687305-132687703 | Common:4; Rare:149; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132828820-132829181 | Common:4; Rare:127 | ||||
| chr12:132887558-132887845 | Rare:82 | ||||
| chr12:132956260-132956437 | Common:1; Rare:36 | ||||
| chr12:132986196-132986442 | Rare:59 | ||||
| chr12:133037220-133037543 | Common:4; Rare:67 | ||||
| chr12:133130238-133130662 | Common:7; Rare:142 |