| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127858075-127858389 | Common:4; Rare:123 | ||||
| chr2:127886412-127886549 | Rare:41 | ||||
| chr2:128027224-128027610 | Common:1; Rare:144 | ||||
| chr2:128028074-128028312 | Common:1; Rare:61 | ||||
| chr2:128090942-128091400 | Common:8; Rare:148 | ||||
| chr2:128318816-128319054 | Common:3; Rare:95 | ||||
| chr2:130158116-130158344 | Rare:66 | ||||
| chr2:130180835-130181131 | Common:2; Rare:72 | ||||
| chr2:130181479-130181819 | Common:4; Rare:155 | ||||
| chr2:130182026-130182277 | Common:1; Rare:85 | ||||
| chr2:130342065-130342318 | Rare:101; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:130342552-130342959 | Common:8; Rare:135 | ||||
| chr2:130355873-130356093 | Common:3; Rare:59 | ||||
| chr2:130371424-130371754 | Common:1; Rare:52 | ||||
| chr2:130371869-130372072 | Common:1; Rare:45 |