chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172914603172914604GA16GENICpossibly homozygous55843676
5172916875172916876CT16GENIChomozygous55843679
5172918510172918511AG11GENIChomozygous55843680
5172919861172919862CG16GENIChomozygous55843681
5172922763172922764GC8GENIChomozygous55843683
5172935682172935683AG13GENIChomozygous55843689
5172936708172936709GA15GENIChomozygous55843690
5172940806172940807AG11GENIChomozygous55843695
5172945848172945849TC14GENIChomozygous55843698
5172947292172947293GT17GENIChomozygous55843699
5172947809172947810GA13GENIChomozygous55843700
5172954250172954251CCCT12GENIChomozygous55843706
5172954699172954700CT15GENIChomozygous55843708
5172955210172955212AC--12GENIChomozygous55843709
5172955239172955240CT16GENIChomozygous55843710
5172957479172957480CG10GENIChomozygous55843712
5172960193172960197TGCT----13GENIChomozygous55843713
5172961683172961684AT12GENIChomozygous55843714
5172962595172962596CA15GENIChomozygous55843715
5172962803172962804TC12GENIChomozygous55843716
5172963621172963622AT18GENIChomozygous55843718
5172963774172963775AG10GENIChomozygous55843719
5172963935172963936GA10GENIChomozygous55843720
5172963959172963961AG--11GENIChomozygous55843721
5172964382172964383CT9GENIChomozygous55843722
5172965528172965529TC17GENIChomozygous55843723
5172965798172965799AC9GENIChomozygous55843724
5172965909172965910TC14GENIChomozygous55843725
5172967694172967695CT11GENIChomozygous55843727
5172968931172968932AG13GENIChomozygous55843728
5172970353172970354GA9GENIChomozygous55843729
5172973386172973387AG11GENIChomozygous55843733
5172974081172974082GA11GENIChomozygous55843735
5172974313172974314TA9GENIChomozygous55843736
5172974920172974921CT10GENIChomozygous55843737
5172977651172977659CACACACA--------8GENIChomozygous55843738
5172977694172977710ACACGCACACACACAT----------------14GENIChomozygous55843739
5172979557172979558AC10GENIChomozygous55843742
5172980663172980664AG20GENIChomozygous55843743