| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238426565-238427109 | Common:8; Rare:156 | ||||
| chr2:238427300-238427423 | Common:1; Rare:33 | ||||
| chr2:239400916-239401142 | Common:3; Rare:72 | ||||
| chr2:239401378-239401475 | Rare:43 | ||||
| chr2:239401584-239402010 | Common:5; Rare:209 | ||||
| chr2:240025280-240025694 | Common:3; Rare:151; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136234-240136544 | Common:2; Rare:115 | ||||
| chr2:240136564-240136662 | Common:2; Rare:15 | ||||
| chr2:240136799-240136906 | Common:3; Rare:26 | ||||
| chr2:240435175-240435356 | Common:1; Rare:78 | ||||
| chr2:240560210-240560455 | Common:2; Rare:97 | ||||
| chr2:240560693-240560931 | Common:2; Rare:120 | ||||
| chr2:240560944-240561377 | Common:4; Rare:217 | ||||
| chr2:240565789-240566081 | Common:3; Rare:62 | ||||
| chr2:240566158-240566273 | Common:1; Rare:21 |