| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48987052-48987221 | Rare:18 | ||||
| chr12:49028873-49029180 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:49060707-49060904 | Common:1; Rare:80 | ||||
| chr12:49234578-49234701 | Rare:37 | ||||
| chr12:49322069-49322171 | Rare:12 | ||||
| chr12:49633533-49633653 | Common:1; Rare:43 | ||||
| chr12:49654190-49654474 | Common:2; Rare:67 | ||||
| chr12:49656407-49656703 | Rare:52 | ||||
| chr12:49719456-49719494 | Rare:5 | ||||
| chr12:49762603-49762957 | Common:1; Rare:91 | ||||
| chr12:49911845-49911973 | Common:1; Rare:14 | ||||
| chr12:50937324-50937462 | Common:2; Rare:27 | ||||
| chr12:51814742-51815052 | Common:2; Rare:76 | ||||
| chr12:52032950-52033237 | Common:1; Rare:83 | ||||
| chr12:52082082-52082170 | Common:2; Rare:19 |