chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG33GENIChomozygous798296870
4140887405140887406GC33GENIChomozygous798296871
4140887526140887527AG21GENIChomozygous798296872
4140889290140889291CA44GENICheterozygous798296873
4140892114140892115TA37GENIChomozygous798296874
4140892182140892183AT38GENICheterozygous798296875
4140894149140894150GA40GENIChomozygous798296876
4140894483140894484TC35GENIChomozygous798296877
4140894658140894659GC45GENIChomozygous798296878
4140896988140896989GA50GENIChomozygous798296879
4140899328140899329GA25GENIChomozygous798296880
4140901019140901020TC29GENICheterozygous798296881
4140902715140902716TC24GENIChomozygous798296882
4140902957140902958AG46GENIChomozygous798296883
4140903807140903808CT24GENIChomozygous798296884
4140904293140904294CG13GENIChomozygous798296885
4140904305140904306TC11GENIChomozygous798296886
4140906395140906396AG33GENIChomozygous798296887
4140907673140907674TC29GENICheterozygous798296888
4140908274140908275TG36GENIChomozygous798296889
4140908994140908995GC24GENIChomozygous798296890
4140909042140909043GA21GENIChomozygous798296891
4140909059140909060CA23GENIChomozygous798296892
4140909109140909110GA20GENIChomozygous798296893
4140909129140909130CT18GENICpossibly homozygous798296894
4140909170140909171GA21GENIChomozygous798296895
4140909196140909197CT32GENICpossibly homozygous798296896
4140909244140909245GT35GENIChomozygous798296897
4140909248140909249TA35GENIChomozygous798296898
4140909269140909270GA32GENIChomozygous798296899
4140909286140909287GC34GENIChomozygous798296900
4140913023140913024AG33GENIChomozygous798296901
4140913522140913523CT19GENIChomozygous798296902
4140916630140916631TG29GENIChomozygous798296903
4140916631140916632CA30GENIChomozygous798296904
4140916937140916938GA36GENIChomozygous798296905