| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238426631-238427081 | Common:7; Rare:200 | ||||
| chr2:238427180-238427710 | Common:9; Rare:207 | ||||
| chr2:238847905-238848132 | Rare:43 | ||||
| chr2:239400980-239401550 | Common:3; Rare:259 | ||||
| chr2:239401570-239401840 | Common:4; Rare:215 | ||||
| chr2:240025291-240025489 | Common:4; Rare:156; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr2:240136239-240136398 | Common:1; Rare:116 | ||||
| chr2:240435039-240435403 | Common:3; Rare:222 | ||||
| chr2:240435459-240435910 | Common:6; Rare:261 | ||||
| chr2:240560140-240560460 | Common:2; Rare:174 | ||||
| chr2:240560450-240560960 | Common:3; Rare:291 | ||||
| chr2:240561018-240561322 | Common:7; Rare:262 | ||||
| chr2:240568341-240568522 | Rare:78 | ||||
| chr2:240568693-240568871 | Common:2; Rare:84 | ||||
| chr2:240586190-240586510 | Common:4; Rare:135 |