| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26033778-26034159 | Common:3; Rare:138 | ||||
| chr2:26034300-26034713 | Common:3; Rare:102 | ||||
| chr2:26244577-26245110 | Common:2; Rare:181; Clinvar:7; Clinvar (benign):9 | ||||
| chr2:26345768-26346206 | Common:1; Rare:132 | ||||
| chr2:26764203-26764385 | Common:2; Rare:66 | ||||
| chr2:27032846-27033149 | Rare:101 | ||||
| chr2:27035611-27035982 | Common:2; Rare:93 | ||||
| chr2:27059095-27059274 | Common:2; Rare:57 | ||||
| chr2:27078247-27079016 | Common:5; Rare:180 | ||||
| chr2:27134615-27134797 | Common:1; Rare:73 | ||||
| chr2:27211762-27212149 | Common:3; Rare:136 | ||||
| chr2:27212225-27212480 | Common:2; Rare:127 | ||||
| chr2:27212956-27213201 | Rare:74 | ||||
| chr2:27217087-27217409 | Common:1; Rare:92 | ||||
| chr2:27322990-27323209 | Common:2; Rare:74; Clinvar (benign):1 |