chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3118318617118318618AG50GENIChomozygous111685729
3118319401118319402CT54GENIChomozygous111685730
3118321233118321234AG51GENIChomozygous111685731
3118322987118322988CT29GENIChomozygous111685732
3118323119118323120CT31GENIChomozygous111685733
3118323662118323663GA44GENICpossibly homozygous111685734
3118325149118325150AG41GENICpossibly homozygous111685735
3118325421118325422GA38GENICheterozygous111685736
3118325918118325919AC32GENIChomozygous111685737
3118326185118326186GA28GENICpossibly homozygous111685738
3118327712118327713CT33GENIChomozygous111685739
3118328012118328013AT35GENIChomozygous111685740
3118329628118329629CA16GENIChomozygous111685741
3118332068118332069GA22GENIChomozygous111685742
3118332083118332084AG21GENIChomozygous111685743
3118333724118333725AT19GENIChomozygous111685744
3118336719118336720GA54GENIChomozygous111685745
3118337149118337150CT32GENIChomozygous111685746
3118339390118339391AG35GENIChomozygous111685747
3118340549118340550TC36GENIChomozygous111685748
3118341308118341309CT41GENIChomozygous111685749
3118342337118342338AG50GENIChomozygous111685750
3118342650118342651AG37GENICheterozygous111685751
3118354288118354289AC29GENIChomozygous111685752
3118354499118354500GA50GENIChomozygous111685753
3118356025118356026AG32GENIChomozygous111685754
3118356605118356606CA47GENIChomozygous111685755
3118357393118357394CT41GENIChomozygous111685756
3118359735118359736CT31GENICheterozygous111685757
3118359754118359755GT37GENIChomozygous111685758
3118359839118359840CT52GENIChomozygous111685759
3118360922118360923CT19GENIChomozygous111685760
3118365098118365099CT17GENICheterozygous111685761
3118368352118368353GA16GENIChomozygous111685762