| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24310302-24310592 | Rare:84 | ||||
| chr2:24824493-24824743 | Common:3; Rare:71 | ||||
| chr2:24826085-24826259 | Common:1; Rare:59 | ||||
| chr2:25420796-25421106 | Common:1; Rare:52 | ||||
| chr2:25810696-25810998 | Common:1; Rare:45 | ||||
| chr2:26191601-26191927 | Common:2; Rare:76 | ||||
| chr2:26193575-26193916 | Rare:100; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr2:27021984-27022322 | Common:2; Rare:62 | ||||
| chr2:27025341-27025606 | Common:1; Rare:57 | ||||
| chr2:27025612-27025907 | Common:2; Rare:75 | ||||
| chr2:27053764-27053950 | Rare:46 | ||||
| chr2:27079073-27079189 | Rare:42; Clinvar:1 | ||||
| chr2:27215490-27215714 | Rare:67 | ||||
| chr2:27375364-27375623 | Rare:75 | ||||
| chr2:27375707-27375970 | Common:1; Rare:103 |