| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:990425-990580 | Common:1; Rare:39 | ||||
| chr12:990729-990868 | Rare:41 | ||||
| chr12:991095-991347 | Common:4; Rare:109 | ||||
| chr12:1593049-1593152 | Rare:24 | ||||
| chr12:1593153-1593177 | Rare:7 | ||||
| chr12:1690839-1691117 | Common:3; Rare:107 | ||||
| chr12:1691140-1691432 | Common:2; Rare:78 | ||||
| chr12:2004376-2004669 | Common:2; Rare:104 | ||||
| chr12:2053474-2053595 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:2794864-2795238 | Common:1; Rare:129 | ||||
| chr12:2795826-2796054 | Common:1; Rare:65 | ||||
| chr12:2796696-2797230 | Common:2; Rare:112 | ||||
| chr12:2812607-2812733 | Common:1; Rare:45 | ||||
| chr12:2812885-2812945 | Rare:23 | ||||
| chr12:2823544-2823861 | Rare:89 |