chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135481989135481990CT18GENICheterozygous72086477
4135482066135482067CT14GENIChomozygous72086479
4135482431135482432AG22GENIChomozygous72086481
4135482690135482691CA26GENIChomozygous71157832
4135483979135483980TC14GENIChomozygous72086483
4135484128135484129TG17GENIChomozygous72086485
4135484187135484188TA19GENICheterozygous72086487
4135484310135484311TC16GENIChomozygous71157835
4135484866135484867TC29GENICpossibly homozygous72086489