chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25910417559104176CT32GENIChomozygous73634938
25910596159105962GA31GENIChomozygous73634941
25910758959107590CT25GENICpossibly homozygous73634944
25910790659107907GT25GENIChomozygous73634947
25910791059107911CT25GENIChomozygous73634950
25910917159109172AT26GENIChomozygous73634953
25910971959109720GA28GENIChomozygous73634956
25911056459110565CG32GENIChomozygous73634959
25911060459110605GA33GENIChomozygous73634962
25911094459110945CG17GENIChomozygous73634965
25911117159111172AG25GENIChomozygous73634971
25911142659111427GA22GENIChomozygous73634974
25911161059111611CT38GENIChomozygous73634977
25911174159111742AC21GENIChomozygous73634980
25911194359111944GA12GENIChomozygous73634986
25911199959112000TC16GENIChomozygous73634992
25911208259112083AG24GENIChomozygous73634995
25911230359112304CT31GENIChomozygous73634998
25911347059113471CA32GENIChomozygous73635001
25911380359113804GA27GENIChomozygous73635004
25911458259114583CT29GENIChomozygous73635007
25911468159114682AG42GENIChomozygous73635010
25911514559115146AT41GENIChomozygous73635013
25911526959115270TC22GENIChomozygous73635016
25911529159115292CA21GENIChomozygous73635019
25911548059115481AG12GENIChomozygous73635022
25911611059116111CT21GENIChomozygous73635025
25911680759116808CT14GENIChomozygous73635028
25911714459117145CA29GENIChomozygous73635031
25911873959118740AC34GENIChomozygous73635034
25912146659121467AG24GENICpossibly homozygous73635037
25912404459124045CT31GENIChomozygous73635043
25912515159125152GA27GENIChomozygous73635046
25912602459126025TC21GENIChomozygous73635049
25912703259127033TA32GENICheterozygous73635058
25912715759127158GA31GENIChomozygous73635061