chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4123645977123645978TC14GENIChomozygous143156324
4123646278123646279GA13GENIChomozygous143156325
4123646702123646703AG17GENIChomozygous143156326
4123648094123648107TCACACAGCTCGT18GENIChomozygous143062088
4123648193123648194CT23GENIChomozygous143156327
4123648456123648457CT17GENIChomozygous143156328
4123648989123648990GA10GENIChomozygous143156329
4123649049123649050GA11GENIChomozygous143156330
4123649985123649986AG24GENIChomozygous143156331
4123650561123650562TA25GENIChomozygous143156332
4123651515123651516TA24GENIChomozygous143156333
4123651718123651719GT20GENIChomozygous143156334
4123653259123653259G26GENIChomozygous143062089
4123653506123653507G20GENIChomozygous143062090
4123653507123653508GT20GENIChomozygous143156335
4123653511123653512GA20GENIChomozygous143156336
4123654824123654825TC12GENIChomozygous143156337
4123658379123658380AG22GENIChomozygous143156338
4123664589123664590GA26GENIChomozygous143156339
4123665610123665611GA18GENIChomozygous143156340
4123666688123666689CG25GENIChomozygous143156341
4123662355123662355AC14GENICpossibly homozygous143932014