| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3873355-3873514 | Common:1; Rare:36 | ||||
| chr12:4320949-4321255 | Common:5; Rare:116 | ||||
| chr12:4538444-4538940 | Common:3; Rare:112 | ||||
| chr12:4649045-4649149 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr12:6444838-6445047 | Common:1; Rare:35 | ||||
| chr12:6493234-6493394 | Common:6; Rare:44 | ||||
| chr12:6493545-6493604 | Common:2; Rare:9 | ||||
| chr12:6493725-6494154 | Common:2; Rare:126 | ||||
| chr12:6534389-6534659 | Common:5; Rare:108 | ||||
| chr12:6568260-6568371 | Rare:42 | ||||
| chr12:6607369-6607690 | Common:5; Rare:51 | ||||
| chr12:6631634-6631705 | Common:1; Rare:17 | ||||
| chr12:6635932-6636086 | Common:2; Rare:43 | ||||
| chr12:6689381-6689748 | Common:3; Rare:97 | ||||
| chr12:6723830-6724142 | Common:1; Rare:65 |