chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95308432453084325AG20GENICpossibly homozygous812990547
95308559153085592CT19GENIChomozygous812990548
95308841053088411CT12GENIChomozygous812990549
95308968253089683GA6GENIChomozygous812990550
95308995553089956AC32GENIChomozygous812990551
95309077953090780CG26GENIChomozygous812990552
95309142953091430GA20GENIChomozygous812990553
95309166253091663CT34GENIChomozygous812990554
95309201053092011GT25GENIChomozygous812990555
95309469753094698TA13GENIChomozygous812990556
95309615153096152CT26GENIChomozygous812990557
95309658153096582TC9GENIChomozygous812990558