| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:54973339-54973875 | Common:4; Rare:164 | ||||
| chr2:54974041-54974377 | Common:2; Rare:64 | ||||
| chr2:54974390-54974788 | Rare:119 | ||||
| chr2:54987293-54987614 | Common:1; Rare:75 | ||||
| chr2:55048974-55049000 | Rare:7 | ||||
| chr2:55049148-55049326 | Rare:45 | ||||
| chr2:55049752-55050614 | Common:7; Rare:284 | ||||
| chr2:55231703-55232041 | Common:1; Rare:84 | ||||
| chr2:55232242-55232810 | Common:5; Rare:172 | ||||
| chr2:55233774-55234048 | Common:3; Rare:66 | ||||
| chr2:55268687-55268981 | Common:2; Rare:65 | ||||
| chr2:55519411-55519876 | Common:2; Rare:154 | ||||
| chr2:55543814-55543996 | Common:2; Rare:48 | ||||
| chr2:55618849-55618905 | Rare:19 | ||||
| chr2:55693789-55693935 | Rare:60; Clinvar (benign):2 |