| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237601617-237601716 | Rare:24 | ||||
| chr2:238060741-238061135 | Common:6; Rare:123 | ||||
| chr2:238203583-238203789 | Common:3; Rare:84 | ||||
| chr2:240025282-240025455 | Common:1; Rare:69; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136274-240136404 | Common:1; Rare:60 | ||||
| chr2:240560760-240560873 | Common:1; Rare:49 | ||||
| chr2:240868495-240868640 | Common:2; Rare:24 | ||||
| chr2:240868683-240869262 | Common:13; Rare:174; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):19 | ||||
| chr2:240871160-240871449 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr2:240876544-240876668 | Common:1; Rare:19 | ||||
| chr2:241102263-241102500 | Common:2; Rare:75 | ||||
| chr2:241239747-241240387 | Common:1; Rare:174 | ||||
| chr2:241255049-241255578 | Common:1; Rare:118 | ||||
| chr2:241256340-241256808 | Common:2; Rare:113 | ||||
| chr2:241272782-241272988 | Rare:75 |