| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108983375-108983483 | Common:2; Rare:14 | ||||
| chr12:109110983-109111250 | Common:1; Rare:76; Clinvar:1 | ||||
| chr12:109228737-109228829 | Rare:15 | ||||
| chr12:109310479-109310508 | Common:1; Rare:8 | ||||
| chr12:109359408-109359534 | Rare:23 | ||||
| chr12:109619154-109619288 | Common:1; Rare:31 | ||||
| chr12:109625166-109625320 | Rare:30 | ||||
| chr12:109735670-109735824 | Common:1; Rare:25 | ||||
| chr12:109736686-109736848 | Common:1; Rare:38 | ||||
| chr12:109845431-109845585 | Common:1; Rare:31 | ||||
| chr12:109881392-109881476 | Rare:11 | ||||
| chr12:110339118-110339564 | Common:2; Rare:83; Clinvar (benign):1 | ||||
| chr12:110510613-110510652 | Rare:11 | ||||
| chr12:110522065-110522310 | Common:1; Rare:54 | ||||
| chr12:110649431-110649614 | Common:1; Rare:43 |