chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135481340135481341AG44GENICheterozygous71157829
4135481989135481990CT51GENICpossibly homozygous72086477
4135482066135482067CT42GENIChomozygous72086479
4135482431135482432AG58GENICpossibly homozygous72086481
4135482690135482691CA66GENIChomozygous71157832
4135483979135483980TC49GENIChomozygous72086483
4135484128135484129TG42GENICpossibly homozygous72086485
4135484187135484188TA43GENIChomozygous72086487
4135484310135484311TC69GENICpossibly homozygous71157835
4135484866135484867TC36GENIChomozygous72086489