| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:234496462-234496938 | Common:2; Rare:131 | ||||
| chr2:234497039-234497371 | Common:6; Rare:100 | ||||
| chr2:236569571-236569872 | Common:8; Rare:55 | ||||
| chr2:237085761-237085951 | Common:2; Rare:69 | ||||
| chr2:237414079-237414391 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr2:237692372-237692520 | Rare:44 | ||||
| chr2:238060719-238061115 | Common:6; Rare:128 | ||||
| chr2:238107683-238107822 | Rare:42 | ||||
| chr2:238203591-238203797 | Common:3; Rare:88 | ||||
| chr2:238426893-238427067 | Common:1; Rare:65 | ||||
| chr2:239401641-239401781 | Rare:72 | ||||
| chr2:240025261-240025480 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136264-240136439 | Common:1; Rare:78 | ||||
| chr2:240560732-240560873 | Common:1; Rare:65 | ||||
| chr2:240561054-240561326 | Common:4; Rare:120 |