chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5149176158149176159CT18GENIChomozygous55787915
5149176296149176297GC16GENIChomozygous55787917
5149176474149176475CT26GENIChomozygous55787919
5149177777149177778GGTTTATTTA13GENIChomozygous55787921
5149178009149178010CCT10GENIChomozygous55787924
5149178214149178215CCT8GENICheterozygous55787926
5149178214149178215CCTT8GENICpossibly homozygous55787928
5149179256149179257CCT19GENIChomozygous55787932
5149179751149179767GTGTGTGTGTGTGTGT----------------9GENIChomozygous55787936
5149181470149181471A-2GENIChomozygous55787944
5149181586149181587GT24GENIChomozygous55787946
5149182069149182070C-5GENICheterozygous55787948
5149182767149182768AG27GENIChomozygous55787950
5149183723149183724TC20GENIChomozygous55787952
5149183999149184000CCATTTGCGG29GENIChomozygous55787954
5149184101149184102G-28GENIChomozygous55787956
5149184142149184143AAT28GENIChomozygous55787958
5149184577149184578AATGTGTG6GENIChomozygous56460166
5149184794149184795CG23GENIChomozygous55787960
5149184987149184988TTGCGTGTGC5GENICheterozygous56460167
5149185077149185078CT15GENIChomozygous55787966
5149185520149185521CT16GENIChomozygous55787968
5149185879149185880CT16GENIChomozygous55787970
5149185999149186000GA17GENIChomozygous55787972
5149186091149186092CG11GENIChomozygous55787974
5149186092149186093CG11GENIChomozygous55787976
5149186093149186094CA11GENIChomozygous55787978
5149186243149186244G-17GENIChomozygous55787980
5149186980149186986TGTGTG------3GENIChomozygous56460169
5149187532149187534AT--54GENIChomozygous55787990
5149187902149187904GT--40GENIChomozygous55787992
5149187943149187944GGTGTA54GENICpossibly homozygous55787994
5149188014149188015AAG41GENIChomozygous55787998
5149188042149188043GT42GENIChomozygous55788000
5149188067149188068TG42GENIChomozygous55788002
5149188070149188071CA40GENIChomozygous55788004
5149188838149188839TC29GENIChomozygous55788006