chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157420009157420010AG31GENIChomozygous108325688
1157424458157424459TC16GENIChomozygous108325690
1157425460157425461GA26GENIChomozygous108325692
1157427690157427691GA28GENIChomozygous108325694
1157433759157433760TG6GENIChomozygous120811240
1157434696157434697TG15GENICpossibly homozygous108325696
1157435241157435242GA21GENIChomozygous108325698
1157437225157437226CT31GENIChomozygous108325700
1157438859157438860TA28GENIChomozygous108325702
1157443190157443191TC24GENIChomozygous108325708
1157446112157446113CT28GENIChomozygous108325710
1157451627157451628CT19GENIChomozygous108325712
1157453877157453878GA26GENIChomozygous108325714
1157460280157460281TC35GENIChomozygous108325718