chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101106130711061307TACA53GENIChomozygous131463099
101106186811061869CA37GENICpossibly homozygous116993919
101106196111061962CT41GENIChomozygous116993920
101106235711062358CA41GENIChomozygous116494111
101106368711063688AC41GENICpossibly homozygous116494117
101106429511064296GA36GENIChomozygous116494119
101106531211065313GT35GENIChomozygous116993921
101106640711066408CT43GENIChomozygous116993922
101106672611066727AC41GENIChomozygous116494129
101106765411067655AG39GENIChomozygous116494133
101106769011067691AG46GENIChomozygous116494135
101106843011068431TC60GENIChomozygous116494139
101106962011069621GA48GENIChomozygous116494145
101107260711072647GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGC40GENIChomozygous131463100
101107370011073701GA50GENIChomozygous116993923
101107528111075282CT55GENIChomozygous116993924
101107858911078590AG52GENIChomozygous116494169
101106894511068946CA11GENIChomozygous117981276
101108015611080207AAAACACACACACACACACACACACACACACACACACACACACACACACAC14GENICheterozygous128789634
101108081311080814CT60GENIChomozygous116494179
101108116211081162GG58GENIChomozygous128789636
101108121711081218GC67GENIChomozygous116734216
101108252211082523CT38GENIChomozygous116993925
101108274811082749AG54GENIChomozygous116494187
101108446411084465GA46GENIChomozygous116494189
101108494611084947CA44GENIChomozygous117248550
101108412511084126TC40GENIChomozygous117248548