chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95308559153085592CT31GENIChomozygous958645446
95308763053087631TC20GENIChomozygous958645447
95308841053088411CT23GENIChomozygous958645448
95308889253088893AT8GENIChomozygous958645449
95308968253089683GA9GENIChomozygous958645450
95308995553089956AC20GENIChomozygous958645451
95309077953090780CG17GENIChomozygous958645452
95309142953091430GA30GENIChomozygous958645453
95309166253091663CT26GENIChomozygous958645454
95309201053092011GT24GENIChomozygous958645455
95309469753094698TA21GENIChomozygous958645456
95309615153096152CT28GENIChomozygous958645457
95309658153096582TC20GENIChomozygous958645458