| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238238934-238239810 | Common:2; Rare:469 | ||||
| chr2:238239899-238240299 | Common:7; Rare:348 | ||||
| chr2:238288635-238289420 | Common:1; Rare:684 | ||||
| chr2:238320223-238320685 | Common:4; Rare:312 | ||||
| chr2:238426110-238426510 | Common:1; Rare:71 | ||||
| chr2:238426476-238427250 | Common:39; Rare:970 | ||||
| chr2:238427182-238427582 | Common:6; Rare:152 | ||||
| chr2:239400939-239401916 | Common:36; Rare:1873 | ||||
| chr2:240025203-240025680 | Common:15; Rare:701; Clinvar:28; Clinvar (benign):24; Clinvar (pathogenic):7 | ||||
| chr2:240136051-240136451 | Common:6; Rare:419 | ||||
| chr2:240136480-240136750 | Common:4; Rare:63 | ||||
| chr2:240435073-240435873 | Common:7; Rare:462 | ||||
| chr2:240452632-240452817 | Common:2; Rare:70 | ||||
| chr2:240560086-240561356 | Common:44; Rare:2547 | ||||
| chr2:240561621-240562122 | Common:6; Rare:196 |