chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124959001124959002CT52GENICpossibly homozygous116083623
7124959159124959160AG70GENICpossibly homozygous116083624
7124960248124960249TC42GENIChomozygous116083625
7124960521124960522CT36GENICpossibly homozygous116083626
7124960537124960538GA37GENIChomozygous116083627
7124961407124961408TC50GENIChomozygous116083628
7124961670124961671AG43GENICheterozygous116083629
7124961672124961673CT43GENICheterozygous116083630
7124961690124961691AG44GENIChomozygous116083631
7124961692124961693CT43GENICpossibly homozygous116083632
7124961727124961728GA50GENIChomozygous116083633
7124962937124962938TC24GENIChomozygous116083634
7124963035124963036AG46GENIChomozygous116083635
7124963803124963804GA50GENIChomozygous116083636
7124963917124963918TC46GENICpossibly homozygous116083637
7124964052124964053AG32GENIChomozygous116083638
7124962933124962934AG22GENIChomozygous115868140
7124969582124969583CA52GENICpossibly homozygous116083639
7124972945124972946AG56GENIChomozygous115868202
7124973199124973200TC64GENIChomozygous115868206
7124973279124973280CT61GENIChomozygous115868208
7124974291124974292CT51GENIChomozygous115868210
7124974423124974424AT37GENIChomozygous115868212
7124974916124974917CT47GENICpossibly homozygous116083640
7124975142124975143AT30GENICpossibly homozygous116083641
7124975233124975234GA34GENIChomozygous115868214
7124975848124975849GC57GENIChomozygous115868216
7124975867124975868TC50GENIChomozygous116083642
7124976368124976369AG38GENIChomozygous115868218
7124977143124977144CT43GENIChomozygous116083643
7124977641124977642GA73GENIChomozygous115868222
7124977821124977822GA60GENIChomozygous116083644
7124977848124977849CT52GENICpossibly homozygous115868224
7124977952124977953CT65GENIChomozygous116083645
7124978140124978141TC36GENICpossibly homozygous115868228
7124978196124978197AC34GENICheterozygous116394022
7124980498124980499CG43GENIChomozygous116227063
7124981010124981011CT56GENICpossibly homozygous115868232
7124982379124982380AG31GENIChomozygous115868234