| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238239868-238240331 | Common:7; Rare:335 | ||||
| chr2:238288518-238289215 | Common:1; Rare:464 | ||||
| chr2:238320206-238320613 | Common:4; Rare:257 | ||||
| chr2:238426450-238427093 | Common:15; Rare:351 | ||||
| chr2:239400883-239401494 | Common:6; Rare:375 | ||||
| chr2:239401591-239401836 | Common:3; Rare:257 | ||||
| chr2:240025227-240025621 | Common:10; Rare:324; Clinvar:12; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr2:240135980-240136180 | Common:7; Rare:83 | ||||
| chr2:240136201-240136763 | Common:9; Rare:370 | ||||
| chr2:240136730-240137050 | Common:3; Rare:72 | ||||
| chr2:240435137-240435884 | Common:7; Rare:534 | ||||
| chr2:240452559-240452952 | Common:8; Rare:314 | ||||
| chr2:240454640-240454809 | Common:1; Rare:45 | ||||
| chr2:240457653-240457853 | Common:4; Rare:47 | ||||
| chr2:240560197-240560527 | Common:4; Rare:263 |