| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:217903975-217904252 | Common:1; Rare:52 | ||||
| chr2:217905391-217905587 | Rare:39 | ||||
| chr2:217937517-217937624 | Rare:21 | ||||
| chr2:217978639-217978755 | Rare:35 | ||||
| chr2:217978770-217979206 | Common:4; Rare:121 | ||||
| chr2:218217064-218217226 | Common:1; Rare:61 | ||||
| chr2:218245238-218245513 | Rare:49 | ||||
| chr2:218270095-218270601 | Common:5; Rare:163; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:218287250-218287427 | Common:1; Rare:30 | ||||
| chr2:218292482-218292685 | Common:1; Rare:61 | ||||
| chr2:218322986-218323300 | Common:6; Rare:104 | ||||
| chr2:218398546-218398767 | Common:4; Rare:82 | ||||
| chr2:218399528-218399760 | Common:1; Rare:105 | ||||
| chr2:218400480-218400607 | Common:3; Rare:41 | ||||
| chr2:218568276-218568640 | Common:3; Rare:98 |