chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98457138784571388AC29GENICpossibly homozygous117750964
98457147384571474GA32GENIChomozygous117750965
98457285384572854TG20GENICpossibly homozygous117750966
98457394884573949GA25GENIChomozygous117750967
98457518584575186GA12GENIChomozygous117750968
98457561884575619GC35GENICpossibly homozygous117750969
98457589484575895GC28GENIChomozygous117750970
98457668184576682GT26GENIChomozygous117750971
98457722884577229AG15GENICpossibly homozygous117750972
98457756684577567GA20GENIChomozygous117750973
98457845084578451CT24GENIChomozygous117750974
98458010184580102CT26GENIChomozygous117750975
98458327584583276AG35GENIChomozygous117750976
98458335184583352TG19GENIChomozygous117750977
98458353984583540AG17GENIChomozygous117750978
98458357684583577CG20GENIChomozygous117750979
98458359084583591TC18GENIChomozygous117750981
98458363484583635TC22GENIChomozygous117750982
98458418084584181TC18GENIChomozygous117750983
98458630584586306CA28GENIChomozygous117750984
98458706084587061CT10GENIChomozygous117750985
98458726584587266AG14GENICpossibly homozygous117750986
98458766284587663TC21GENIChomozygous117750987
98458823184588232GA18GENIChomozygous117750988
98458941484589415GA15GENIChomozygous117750989
98458955684589557AC23GENIChomozygous117750990
98459298584592986TC28GENICpossibly homozygous117750991
98459351884593519TC21GENIChomozygous117750992
98457296484572965TC17GENIChomozygous117382804
98457298884572989TC14GENIChomozygous117382805
98457314684573147GT8GENIChomozygous120402139