chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101072625210726253CA31GENIChomozygous116493625
101072738510727386AG54GENIChomozygous116493627
101073243610732437TC40GENIChomozygous116493631
101073320110733202AG32GENIChomozygous118079134
101073324610733247GA27GENIChomozygous117191243
101073345710733458CA60GENIChomozygous116734058
101073374410733745TA58GENIChomozygous116734059
101073388110733882TC59GENIChomozygous116993876
101073436610734367GA36GENIChomozygous116734060
101073436810734369TA38GENIChomozygous116734061
101074009410740095AG33GENIChomozygous116734062
101074262010742621AG40GENIChomozygous116734063
101074340710743408GA46GENIChomozygous116493637
101074463710744638AT54GENIChomozygous116858592
101074465210744653GC54GENIChomozygous116493639
101074471310744714CG50GENIChomozygous116734064
101074495710744958AG42GENIChomozygous116734065
101074503310745034TC31GENIChomozygous116734066
101074614010746141CT54GENIChomozygous116734067
101075092310750924GA49GENIChomozygous116734068
101075204310752044CA6GENICheterozygous117150667
101075320310753204GA55GENIChomozygous116734069
101075335610753357AG55GENIChomozygous116734070
101075342210753423TA61GENICpossibly homozygous116734071
101075342510753426CG63GENIChomozygous116734072
101075600810756009GA54GENIChomozygous116493645
101075744210757443GC38GENIChomozygous116493649
101075867410758675TC51GENICpossibly homozygous116734074
101075873710758738CG56GENIChomozygous116493651