| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238426892-238427067 | Common:1; Rare:65 | ||||
| chr2:239401640-239401739 | Rare:46 | ||||
| chr2:240025291-240025488 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136243-240136411 | Common:1; Rare:76 | ||||
| chr2:240560766-240560886 | Common:1; Rare:53 | ||||
| chr2:241102259-241102406 | Common:2; Rare:52 | ||||
| chr2:241149450-241149564 | Common:1; Rare:33 | ||||
| chr2:241272794-241272907 | Rare:42 | ||||
| chr2:241315127-241315406 | Common:5; Rare:90 | ||||
| chr2:241315641-241316186 | Common:5; Rare:200 | ||||
| chr2:241508546-241508816 | Common:1; Rare:85 | ||||
| chr2:241637574-241637704 | Common:1; Rare:75 | ||||
| chr2:241686785-241687124 | Common:4; Rare:101 | ||||
| chr2:241701890-241702067 | Common:1; Rare:73 | ||||
| chr20:325196-325540 | Rare:103 |