| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50456072-50456152 | Common:1; Rare:18 | ||||
| chr12:51240655-51241111 | Rare:106 | ||||
| chr12:51913281-51913580 | Common:4; Rare:89; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:52032950-52033188 | Common:1; Rare:63 | ||||
| chr12:52079838-52080060 | Common:2; Rare:52 | ||||
| chr12:52082075-52082455 | Common:4; Rare:75 | ||||
| chr12:52147301-52147571 | Common:2; Rare:64 | ||||
| chr12:52235655-52235780 | Common:2; Rare:19 | ||||
| chr12:53068261-53068403 | Rare:29 | ||||
| chr12:53665068-53665268 | Rare:28 | ||||
| chr12:56133463-56133626 | Rare:36 | ||||
| chr12:56169583-56169801 | Rare:63 | ||||
| chr12:56169870-56170200 | Rare:84 | ||||
| chr12:56599819-56600080 | Common:2; Rare:67 | ||||
| chr12:56634966-56635116 | Common:1; Rare:27 |