chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124959001124959002CT49GENIChomozygous116083623
7124959159124959160AG49GENIChomozygous116083624
7124960248124960249TC56GENIChomozygous116083625
7124960521124960522CT54GENIChomozygous116083626
7124960537124960538GA49GENIChomozygous116083627
7124961407124961408TC60GENIChomozygous116083628
7124961670124961671AG42GENICheterozygous116083629
7124961672124961673CT45GENICheterozygous116083630
7124961690124961691AG45GENIChomozygous116083631
7124961692124961693CT44GENICpossibly homozygous116083632
7124961727124961728GA67GENIChomozygous116083633
7124962933124962934AG48GENIChomozygous115868140
7124962937124962938TC46GENIChomozygous116083634
7124963035124963036AG53GENIChomozygous116083635
7124963803124963804GA58GENIChomozygous116083636
7124963917124963918TC47GENIChomozygous116083637
7124964052124964053AG42GENIChomozygous116083638
7124969582124969583CA68GENICpossibly homozygous116083639
7124972945124972946AG51GENIChomozygous115868202
7124973199124973200TC63GENIChomozygous115868206
7124973279124973280CT43GENIChomozygous115868208
7124974291124974292CT59GENIChomozygous115868210
7124974423124974424AT50GENIChomozygous115868212
7124974916124974917CT51GENIChomozygous116083640
7124975142124975143AT43GENIChomozygous116083641
7124975233124975234GA56GENICpossibly homozygous115868214
7124975848124975849GC59GENIChomozygous115868216
7124975867124975868TC56GENIChomozygous116083642
7124976368124976369AG53GENIChomozygous115868218
7124977143124977144CT90GENIChomozygous116083643
7124977641124977642GA57GENIChomozygous115868222
7124977821124977822GA47GENIChomozygous116083644
7124977848124977849CT50GENIChomozygous115868224
7124977952124977953CT53GENIChomozygous116083645
7124978140124978141TC52GENIChomozygous115868228
7124980212124980213AG66GENIChomozygous116083646
7124981010124981011CT43GENICpossibly homozygous115868232
7124982379124982380AG49GENIChomozygous115868234