chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12212606722126068TC35GENIChomozygous108695852
12212761022127611GA27GENIChomozygous108836544
12212843922128440GA15GENIChomozygous108836545
12212887022128871TC16GENIChomozygous108695854
12212943522129436AC17GENIChomozygous108695855
12213009922130100TC24GENIChomozygous108695856
12213171422131715GA35GENIChomozygous108836546
12213225022132251CA26GENIChomozygous108836547
12213459222134593AG20GENIChomozygous108695864
12213585122135852GA14GENIChomozygous108836548
12213622722136228AG20GENIChomozygous108695869
12213877822138779TC31GENIChomozygous108695877
12214062122140622AT23GENIChomozygous108695879
12214084122140842TC22GENIChomozygous108695880
12214137422141375TC16GENIChomozygous108695881
12214148722141488GC25GENIChomozygous108836549
12214291522142916CT22GENIChomozygous108836550
12214337122143372GA28GENIChomozygous108836551
12214478622144787GA26GENIChomozygous108836552
12214729422147295AG27GENIChomozygous108695890
12215065822150659TC22GENIChomozygous108695894
12215819422158195GA21GENIChomozygous108836555
12215835822158359TC19GENIChomozygous108695904
12215840722158408CT17GENIChomozygous108836556
12215926822159269CT22GENIChomozygous108836557
12215948422159485TG18GENIChomozygous108695906
12215954522159546CG27GENIChomozygous108836558