| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:19228221-19228621 | Common:4; Rare:89 | ||||
| chr2:19228710-19229080 | Common:2; Rare:67 | ||||
| chr2:19347960-19348182 | Common:1; Rare:85 | ||||
| chr2:19989252-19989499 | Common:3; Rare:59; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:20049643-20049745 | Common:2; Rare:17 | ||||
| chr2:20148678-20148838 | Rare:22 | ||||
| chr2:20148910-20149300 | Common:1; Rare:73 | ||||
| chr2:20196797-20197197 | Common:7; Rare:131 | ||||
| chr2:20374984-20375134 | Rare:56 | ||||
| chr2:20375266-20375445 | Common:2; Rare:34 | ||||
| chr2:20474549-20474715 | Rare:37 | ||||
| chr2:20593347-20593890 | Common:11; Rare:143 | ||||
| chr2:20600113-20600349 | Common:1; Rare:40 | ||||
| chr2:23285410-23285710 | Common:1; Rare:44 | ||||
| chr2:23404503-23404903 | Common:3; Rare:123 |