chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83197737431977375GA15GENIChomozygous116447925
83197788931977890CT9GENIChomozygous116447926
83197795531977956GA8GENIChomozygous116447927
83197799031977991GA14GENIChomozygous116447928
83197818031978181CT15GENIChomozygous116447929
83197824531978246AT20GENIChomozygous116447930
83197840931978410GA13GENIChomozygous116447931
83197862531978626CT24GENIChomozygous116447932
83197869131978692CT15GENIChomozygous116447933
83197870931978710AG19GENIChomozygous116447934
83197887331978874TG10GENIChomozygous116447935
83197906231979063GC21GENIChomozygous116447936
83197915431979155AG24GENIChomozygous116447937
83197919131979192AG21GENIChomozygous116447938
83197924731979248AT22GENIChomozygous116447939
83197934131979342AG23GENIChomozygous116447940
83198012131980122TC18GENIChomozygous116447941
83198024031980241GT18GENIChomozygous116447942
83198076431980765AC15GENIChomozygous116447944
83198085831980859CT23GENIChomozygous116447945
83198130031981301GA14GENIChomozygous116447946
83198135131981352AG20GENIChomozygous116447947
83198153531981536AC23GENIChomozygous116447948
83198158531981586AT22GENIChomozygous116447949
83198391431983915GC19GENIChomozygous116447950
83199052831990529GA22GENIChomozygous116447951
83199140831991409CT23GENICpossibly homozygous116447952
83199190831991909CT31GENIChomozygous116447954
83199222531992226AG32GENIChomozygous116447955
83199310331993104TC17GENIChomozygous116447956
83199397231993973CT20GENIChomozygous116447957
83199993531999936GA15GENIChomozygous116447958