| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26345739-26346195 | Common:4; Rare:272 | ||||
| chr2:26764175-26764351 | Common:4; Rare:135 | ||||
| chr2:26785748-26786127 | Rare:97 | ||||
| chr2:27032801-27033050 | Rare:179 | ||||
| chr2:27051546-27051743 | Rare:112 | ||||
| chr2:27071415-27071877 | Common:3; Rare:222 | ||||
| chr2:27078447-27079017 | Common:7; Rare:263 | ||||
| chr2:27086465-27086855 | Common:12; Rare:217; Clinvar (benign):6 | ||||
| chr2:27093969-27094141 | Common:1; Rare:37 | ||||
| chr2:27148827-27149077 | Rare:52 | ||||
| chr2:27211722-27212154 | Common:6; Rare:280 | ||||
| chr2:27212126-27212439 | Common:5; Rare:288 | ||||
| chr2:27212805-27213337 | Rare:444 | ||||
| chr2:27217248-27217559 | Rare:133 | ||||
| chr2:27262980-27263310 | Common:1; Rare:78 |