chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4123645977123645978TC39GENIChomozygous143156324
4123646278123646279GA45GENIChomozygous143156325
4123646702123646703AG63GENIChomozygous143156326
4123648094123648107TCACACAGCTCGT42GENIChomozygous143062088
4123648193123648194CT49GENIChomozygous143156327
4123648456123648457CT65GENIChomozygous143156328
4123648989123648990GA41GENIChomozygous143156329
4123649049123649050GA56GENIChomozygous143156330
4123649985123649986AG65GENIChomozygous143156331
4123650561123650562TA63GENICpossibly homozygous143156332
4123651515123651516TA63GENIChomozygous143156333
4123651718123651719GT57GENIChomozygous143156334
4123653259123653259G44GENIChomozygous143062089
4123653506123653507G39GENIChomozygous143062090
4123653507123653508GT39GENIChomozygous143156335
4123653511123653512GA39GENIChomozygous143156336
4123654824123654825TC49GENIChomozygous143156337
4123658379123658380AG61GENIChomozygous143156338
4123662355123662355AC38GENICheterozygous143932014
4123664589123664590GA54GENIChomozygous143156339
4123665610123665611GA49GENIChomozygous143156340
4123666688123666689CG69GENIChomozygous143156341