| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534203-6534862 | Common:17; Rare:451 | ||||
| chr12:6563640-6563940 | Common:3; Rare:89 | ||||
| chr12:6568238-6568413 | Rare:120 | ||||
| chr12:6663076-6663403 | Common:3; Rare:171 | ||||
| chr12:6688843-6689196 | Rare:137 | ||||
| chr12:6689220-6689794 | Common:6; Rare:298 | ||||
| chr12:6723828-6724303 | Common:3; Rare:177 | ||||
| chr12:6753020-6753210 | Common:9; Rare:110 | ||||
| chr12:6828286-6828448 | Common:4; Rare:27 | ||||
| chr12:6829190-6829560 | Rare:124 | ||||
| chr12:6829626-6829774 | Common:2; Rare:48 | ||||
| chr12:6851237-6851494 | Rare:120 | ||||
| chr12:6851890-6852203 | Rare:149 | ||||
| chr12:6867361-6867619 | Common:4; Rare:188; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:6867897-6868320 | Common:17; Rare:257 |