| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177536439-177536662 | Common:1; Rare:42 | ||||
| chr2:178379309-178379406 | Common:4; Rare:26 | ||||
| chr2:178413534-178413712 | Common:1; Rare:57 | ||||
| chr2:178413854-178414036 | Common:1; Rare:47 | ||||
| chr2:178418331-178418603 | Common:1; Rare:48 | ||||
| chr2:178428240-178428498 | Common:1; Rare:49 | ||||
| chr2:178436779-178437119 | Common:1; Rare:73 | ||||
| chr2:178437423-178437707 | Rare:50 | ||||
| chr2:178438341-178438373 | Rare:6 | ||||
| chr2:178438825-178438993 | Common:1; Rare:40 | ||||
| chr2:178439337-178439959 | Common:1; Rare:103 | ||||
| chr2:178441655-178441867 | Common:2; Rare:52; Clinvar (benign):2 | ||||
| chr2:179126212-179126646 | Rare:69 | ||||
| chr2:179126670-179126854 | Rare:33 | ||||
| chr2:179263574-179263669 | Common:1; Rare:14 |