chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2046607694660770AG27GENIChomozygous109329613
2046625104662511CG26GENIChomozygous109329615
2047669724766973AG35GENIChomozygous109329617
2047674604767461GA20GENIChomozygous109329619
2047676154767616GT16GENIChomozygous109233604
2047676854767686AG14GENIChomozygous109233605
2047677094767710CG14GENIChomozygous109075193
2047677364767737AC16GENIChomozygous109075197
2047677674767768CG16GENIChomozygous109233606
2047679784767979GC20GENIChomozygous109075215
2047691494769150TC19GENIChomozygous109233608
2047693134769314CT22GENIChomozygous109233609
2047712854771286GC42GENIChomozygous109233612
2047713554771356TG39GENIChomozygous109075223