chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4121342406121342407AC12GENIChomozygous126022807
4121348512121348513TC14GENIChomozygous126022808
4121371957121371958CG3GENICheterozygous126081224
4121373073121373074CA18GENIChomozygous126022809
4121373093121373094TA29GENIChomozygous126022810
4121381589121381590CA6GENICheterozygous126081225
4121381590121381591AC6GENICheterozygous126081226
4121392163121392164TC17GENIChomozygous112824770
4121392170121392171GC13GENIChomozygous112824772
4121392175121392176TC12GENIChomozygous112824774
4121392210121392211TC8GENIChomozygous112824776
4121392217121392218GC7GENIChomozygous112824778
4121392221121392222TC7GENIChomozygous112824780
4121392231121392232CT9GENIChomozygous112824782
4121392256121392257CG18GENIChomozygous112824784
4121410647121410648TC12GENIChomozygous126022811
4121426300121426301CT10GENIChomozygous126022812
4121435836121435837GA4GENIChomozygous112824794
4121471966121471967GA23GENICheterozygous113378144
4121487968121487969TA5GENICheterozygous126081227
4121556036121556037CA3GENICheterozygous126081228
4121563276121563277TA3GENICheterozygous126081229