| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:13980797-13980974 | Common:1; Rare:42 | ||||
| chr12:14365490-14365743 | Common:1; Rare:85 | ||||
| chr12:14774184-14774477 | Common:3; Rare:76 | ||||
| chr12:14803418-14803736 | Common:2; Rare:88 | ||||
| chr12:14885731-14885935 | Common:3; Rare:42; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:15882319-15882587 | Common:1; Rare:70 | ||||
| chr12:16347494-16347732 | Common:4; Rare:45 | ||||
| chr12:16606479-16606652 | Rare:41 | ||||
| chr12:19129436-19129814 | Common:3; Rare:163 | ||||
| chr12:19439364-19439691 | Common:3; Rare:116 | ||||
| chr12:19440578-19440636 | Common:1; Rare:19 | ||||
| chr12:20369490-20369706 | Common:3; Rare:88 | ||||
| chr12:21437616-21437717 | Common:4; Rare:43 | ||||
| chr12:21501556-21501891 | Common:2; Rare:86 | ||||
| chr12:21657749-21658110 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):1 |