| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:232875753-232875887 | Rare:29 | ||||
| chr2:233692721-233692968 | Rare:44 | ||||
| chr2:233728881-233729108 | Common:15; Rare:51 | ||||
| chr2:233760067-233760313 | Common:3; Rare:56; Clinvar:4 | ||||
| chr2:233854423-233854782 | Common:5; Rare:102 | ||||
| chr2:233979975-233980189 | Common:2; Rare:38 | ||||
| chr2:237085761-237085970 | Common:2; Rare:78 | ||||
| chr2:237487141-237487375 | Common:3; Rare:62 | ||||
| chr2:237966728-237967083 | Common:4; Rare:110 | ||||
| chr2:238060732-238061150 | Common:6; Rare:130 | ||||
| chr2:238203554-238203821 | Common:5; Rare:108 | ||||
| chr2:238426892-238427067 | Common:1; Rare:65 | ||||
| chr2:239401641-239401737 | Rare:44 | ||||
| chr2:240025246-240025467 | Common:2; Rare:84; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240560760-240560873 | Common:1; Rare:49 |