| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2877022-2877272 | Rare:78 | ||||
| chr12:2890692-2890941 | Common:1; Rare:101 | ||||
| chr12:3077236-3077438 | Common:7; Rare:88 | ||||
| chr12:3873088-3873182 | Rare:23 | ||||
| chr12:3873355-3873527 | Common:1; Rare:39 | ||||
| chr12:4273583-4273837 | Rare:73 | ||||
| chr12:4320942-4321260 | Common:5; Rare:121 | ||||
| chr12:4538431-4538956 | Common:3; Rare:127 | ||||
| chr12:4648982-4649178 | Common:2; Rare:63; Clinvar (benign):2 | ||||
| chr12:5043797-5044033 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr12:5431929-5432146 | Common:4; Rare:84 | ||||
| chr12:6200230-6200436 | Common:3; Rare:58 | ||||
| chr12:6470623-6470791 | Common:1; Rare:67 | ||||
| chr12:6493230-6493502 | Common:7; Rare:81 | ||||
| chr12:6493763-6494146 | Common:2; Rare:112 |