| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:92962304-92962609 | Common:4; Rare:49 | ||||
| chr1:93017766-93017813 | Rare:9 | ||||
| chr1:93170713-93171003 | Common:2; Rare:64 | ||||
| chr1:93662050-93662106 | Rare:5 | ||||
| chr1:93662620-93662694 | Rare:10 | ||||
| chr1:93848028-93848259 | Common:4; Rare:60 | ||||
| chr1:93878587-93878633 | Rare:7 | ||||
| chr1:94045644-94045932 | Common:2; Rare:72; Clinvar (benign):1 | ||||
| chr1:94048462-94048791 | Common:2; Rare:61 | ||||
| chr1:94048831-94049030 | Common:2; Rare:50; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:94097234-94097413 | Rare:33 | ||||
| chr1:94267022-94267159 | Rare:21 | ||||
| chr1:94417416-94417551 | Rare:22 | ||||
| chr1:94605860-94606133 | Rare:50 | ||||
| chr1:94735372-94735577 | Common:2; Rare:27 |