| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2794873-2795208 | Common:1; Rare:121 | ||||
| chr12:2796703-2796960 | Common:2; Rare:44 | ||||
| chr12:2812559-2812713 | Common:1; Rare:43 | ||||
| chr12:2890653-2890926 | Common:1; Rare:111 | ||||
| chr12:3753064-3753267 | Common:2; Rare:48 | ||||
| chr12:3873113-3873127 | Rare:4 | ||||
| chr12:3873337-3873493 | Common:1; Rare:33 | ||||
| chr12:4273742-4273829 | Rare:23 | ||||
| chr12:4320943-4321260 | Common:5; Rare:121 | ||||
| chr12:4538457-4538923 | Common:2; Rare:101 | ||||
| chr12:4649019-4649149 | Common:2; Rare:45; Clinvar (benign):1 | ||||
| chr12:6451792-6452198 | Common:4; Rare:76 | ||||
| chr12:6493241-6493386 | Common:5; Rare:41 | ||||
| chr12:6534383-6534582 | Common:5; Rare:85 | ||||
| chr12:6548762-6548977 | Common:1; Rare:78 |