| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43637127-43637374 | Common:2; Rare:84 | ||||
| chr2:43676327-43676473 | Common:3; Rare:44 | ||||
| chr2:43773991-43774141 | Common:5; Rare:65; Clinvar (pathogenic):1 | ||||
| chr2:43995811-43995911 | Common:1; Rare:62; Clinvar:6; Clinvar (benign):7 | ||||
| chr2:43995950-43995999 | Common:2; Rare:31; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:43996003-43996315 | Common:3; Rare:125 | ||||
| chr2:44167368-44167529 | Common:1; Rare:35 | ||||
| chr2:44168042-44168236 | Common:1; Rare:73 | ||||
| chr2:44168513-44168920 | Common:1; Rare:124 | ||||
| chr2:44361479-44362122 | Common:4; Rare:212 | ||||
| chr2:45676585-45676754 | Rare:27 | ||||
| chr2:45676896-45677035 | Rare:39 | ||||
| chr2:45977933-45978075 | Common:1; Rare:31 | ||||
| chr2:46297049-46297437 | Common:6; Rare:145 | ||||
| chr2:46429032-46429238 | Common:1; Rare:80 |