chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
33690678336906784T48GENIChomozygous136557399
33691861836918619CG21GENIChomozygous403061865
33691861836918619C21GENICheterozygous403061866
33691863036918631C20GENICheterozygous403061867
33691863036918631CT20GENIChomozygous403061868
33691863336918634C21GENICheterozygous403061869
33695308936953090GC12GENIChomozygous403061870
33695308936953090G12GENICheterozygous403061871
33695327536953276G10GENIChomozygous403061872
33695327536953276GC10GENICheterozygous403061873
33696668436966685G18GENICheterozygous403061875
33696668436966685GC18GENICheterozygous403061876
33696668636966687G18GENICheterozygous403571576
33696668636966687GC18GENICheterozygous403571577
33696668836966689G18GENICheterozygous403983975
33696668836966689GC18GENICheterozygous403983976
33709428837094289GA16GENICpossibly homozygous136679762
33691863336918634CT21GENIChomozygous136679759
33691863636918637CT22GENIChomozygous136679760
33691864036918641CT21GENIChomozygous136679761
33709842137098422TA40GENICheterozygous154088246
33709842137098422T40GENICheterozygous403061877
33712825837128259TG37GENIChomozygous136679763
33712826637128267TC33GENIChomozygous136679764
33712826837128269CT33GENIChomozygous136679765
33712827237128273CT33GENIChomozygous136679766
33712827337128274CA33GENIChomozygous136679767
33712828937128290CT34GENIChomozygous403061878
33712828937128290C34GENICheterozygous403061879
33713521037135211AC14GENIChomozygous403061880
33713521037135211A14GENICheterozygous403061881
33713521637135217AG13GENIChomozygous136679769
33713522437135225AG11GENIChomozygous403061882
33713522437135225A11GENICheterozygous403061883
33713522837135229AG10GENIChomozygous403061884
33713522837135229A10GENICheterozygous403061885
33713523237135233AG10GENIChomozygous403061886
33713523237135233A10GENICheterozygous403061887
33713524037135241A10GENICheterozygous403061891
33713523637135237AG10GENIChomozygous403061888
33713523637135237A10GENICheterozygous403061889
33713524037135241AG10GENIChomozygous403061890