chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117734364117734365CT23GENICheterozygous119407228
4117734526117734527TC10GENICheterozygous112820028
4117734709117734710TC16GENIChomozygous112820030
4117735673117735674CT12GENIChomozygous112820032
4117736257117736258GC13GENIChomozygous119407229
4117736940117736941TC15GENIChomozygous113153251
4117737260117737261CT15GENIChomozygous112820034
4117737883117737884GA18GENIChomozygous113153253
4117738587117738588TG13GENIChomozygous112820036
4117740026117740027CT19GENICpossibly homozygous119527479
4117740390117740391GA23GENIChomozygous119407230
4117740746117740747AG12GENIChomozygous113153257
4117740901117740902GA18GENIChomozygous119527481
4117741295117741296AG18GENIChomozygous112820038
4117741400117741401GA14GENIChomozygous112820040
4117741675117741676AG8GENIChomozygous119407231
4117741799117741800GA12GENIChomozygous119407232
4117742024117742025GA20GENIChomozygous119407233
4117742184117742185AG15GENIChomozygous119407234
4117742578117742579TC16GENIChomozygous112820042
4117742999117743000AG18GENIChomozygous112820044
4117743276117743277TC21GENIChomozygous113153258
4117744154117744155AG6GENIChomozygous113153260
4117744365117744366CT9GENIChomozygous113153261
4117744619117744620GA9GENIChomozygous113153262
4117744879117744880AG5GENIChomozygous113153264
4117745283117745284GC23GENIChomozygous113153265
4117745484117745485TA15GENIChomozygous113153268