chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25910417559104176CT22GENIChomozygous73634938
25910596159105962GA71GENIChomozygous73634941
25910758959107590CT32GENICpossibly homozygous73634944
25910790659107907GT22GENIChomozygous73634947
25910791059107911CT20GENIChomozygous73634950
25910917159109172AT42GENIChomozygous73634953
25910971959109720GA17GENIChomozygous73634956
25911056459110565CG35GENIChomozygous73634959
25911060459110605GA34GENIChomozygous73634962
25911094459110945CG42GENIChomozygous73634965
25911117159111172AG34GENIChomozygous73634971
25911142659111427GA31GENIChomozygous73634974
25911161059111611CT26GENIChomozygous73634977
25911174159111742AC32GENIChomozygous73634980
25911194359111944GA16GENICheterozygous73634986
25911199959112000TC19GENIChomozygous73634992
25911208259112083AG47GENIChomozygous73634995
25911230359112304CT47GENIChomozygous73634998
25911347059113471CA18GENIChomozygous73635001
25911380359113804GA6GENIChomozygous73635004
25911458259114583CT22GENIChomozygous73635007
25911468159114682AG31GENICpossibly homozygous73635010
25911514559115146AT21GENIChomozygous73635013
25911526959115270TC26GENIChomozygous73635016
25911529159115292CA28GENIChomozygous73635019
25911548059115481AG47GENICpossibly homozygous73635022
25911611059116111CT19GENICpossibly homozygous73635025
25911680759116808CT24GENICpossibly homozygous73635028
25911714459117145CA38GENIChomozygous73635031
25911873959118740AC13GENIChomozygous73635034
25912146659121467AG58GENICpossibly homozygous73635037
25912404459124045CT20GENIChomozygous73635043
25912515159125152GA39GENIChomozygous73635046
25912602459126025TC24GENIChomozygous73635049
25912703059127031TA21GENICheterozygous73635055
25912703259127033TA21GENICheterozygous73635058
25912715759127158GA24GENIChomozygous73635061