| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:45567965-45568156 | Common:3; Rare:38 | ||||
| chr2:46616977-46617292 | Common:7; Rare:134; Clinvar (pathogenic):1 | ||||
| chr2:46915742-46915869 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47034071-47034132 | Rare:9 | ||||
| chr2:48314183-48314373 | Common:1; Rare:61 | ||||
| chr2:53786923-53787301 | Common:1; Rare:157 | ||||
| chr2:53970983-53971126 | Common:4; Rare:59 | ||||
| chr2:55232259-55232754 | Common:3; Rare:144 | ||||
| chr2:61017429-61017747 | Common:1; Rare:91; Clinvar:1 | ||||
| chr2:61144950-61145128 | Common:2; Rare:52 | ||||
| chr2:61538038-61538126 | Common:2; Rare:15 | ||||
| chr2:62195979-62196117 | Rare:42 | ||||
| chr2:63588718-63589016 | Rare:92 | ||||
| chr2:63841673-63841898 | Common:1; Rare:81 | ||||
| chr2:64524508-64524602 | Rare:27 |