chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4184947101184947102AG17GENIChomozygous59655810
4184949829184949830TC31GENIChomozygous59655811
4184950060184950061AT31GENIChomozygous59655812
4184950193184950201AGAGAGAG--------22GENIChomozygous59655813
4184950205184950223ACACACAGACACACACAG------------------18GENICpossibly homozygous59655814
4184951415184951459CGCGCACACACACACACACACACACACACACACACACACACACA--------------------------------------------8GENIChomozygous59655815
4184951725184951726TC27GENIChomozygous59655816
4184951788184951789TTGA20GENIChomozygous59655817
4184952358184952359TC36GENIChomozygous59655818
4184954122184954127TTTTT-----17GENICheterozygous59655819
4184957614184957615CCA16GENIChomozygous59655820
4184958701184958702TTACACACACACACAC1GENIChomozygous58568324
4184958874184958875GT14GENIChomozygous59655821
4184960413184960414CT12GENIChomozygous59655822
4184961006184961007G-8GENIChomozygous59655823
4184961008184961009TG10GENIChomozygous59655824
4184961022184961023GC14GENIChomozygous59655825
4184961029184961031AG--14GENIChomozygous59655826
4184961321184961322GC10GENIChomozygous59655827
4184963272184963273GA30GENIChomozygous59655828
4184963308184963309AAAAG26GENICpossibly homozygous59655829
4184963461184963464AGC---18GENIChomozygous59655830
4184963550184963551AG20GENIChomozygous59655831
4184964214184964215AG22GENIChomozygous59655832
4184964303184964304GGGA23GENIChomozygous59655833
4184964563184964564CA21GENICpossibly homozygous59655834
4184964863184964864GT10GENIChomozygous59655835
4184964278184964279T-20GENIChomozygous58516166
4184956821184956822TTAC5GENIChomozygous58360268
4184960580184960581GGCTCTCTCT5GENIChomozygous58360272
4184960382184960384AA--7GENIChomozygous58597640
4184961046184961047GGAC8GENIChomozygous58484096
4184962685184962686AG15GENIChomozygous59440651