| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237414067-237414491 | Common:3; Rare:90; Clinvar (benign):2 | ||||
| chr2:237487136-237487403 | Common:3; Rare:70 | ||||
| chr2:238060738-238061135 | Common:6; Rare:124 | ||||
| chr2:238426655-238427067 | Common:6; Rare:120 | ||||
| chr2:239309178-239309373 | Rare:40 | ||||
| chr2:239401641-239401739 | Rare:45 | ||||
| chr2:240025282-240025456 | Common:1; Rare:69; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136264-240136422 | Common:1; Rare:69 | ||||
| chr2:240560732-240560873 | Common:1; Rare:65 | ||||
| chr2:240561036-240561099 | Common:1; Rare:40 | ||||
| chr2:241102274-241102508 | Common:2; Rare:68 | ||||
| chr2:241188474-241188765 | Common:2; Rare:79 | ||||
| chr2:241272789-241273016 | Rare:80 | ||||
| chr2:241315140-241315414 | Common:5; Rare:93 | ||||
| chr2:241315633-241316195 | Common:5; Rare:204 |