chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4123645977123645978TC14GENIChomozygous143156324
4123646278123646279GA16GENIChomozygous143156325
4123646702123646703AG21GENIChomozygous143156326
4123648094123648107TCACACAGCTCGT15GENIChomozygous143062088
4123648193123648194CT26GENIChomozygous143156327
4123648456123648457CT20GENIChomozygous143156328
4123648989123648990GA10GENIChomozygous143156329
4123649049123649050GA13GENIChomozygous143156330
4123649985123649986AG28GENIChomozygous143156331
4123650561123650562TA19GENIChomozygous143156332
4123651515123651516TA24GENIChomozygous143156333
4123651718123651719GT12GENIChomozygous143156334
4123653259123653259G16GENIChomozygous143062089
4123653506123653507G15GENIChomozygous143062090
4123653507123653508GT15GENIChomozygous143156335
4123653511123653512GA15GENIChomozygous143156336
4123654824123654825TC15GENIChomozygous143156337
4123658379123658380AG17GENIChomozygous143156338
4123664589123664590GA20GENIChomozygous143156339
4123665610123665611GA29GENIChomozygous143156340
4123666688123666689CG20GENIChomozygous143156341