chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1269285578269285579GA19GENIChomozygous61643951
1269286214269286215TC29GENIChomozygous61643952
1269286960269286970GTGTACGTCC----------24GENIChomozygous61643953
1269287148269287149TC39GENIChomozygous61643954
1269287497269287498CCGT9GENICheterozygous61210794
1269287497269287498CCGTGT9GENICpossibly homozygous61210796
1269287963269287964CT35GENIChomozygous61643955
1269288229269288230CT29GENIChomozygous61643956
1269288322269288323AG42GENIChomozygous61643957
1269288942269288943AG23GENIChomozygous61210800
1269289127269289128TC18GENIChomozygous61643958
1269289257269289258TC26GENIChomozygous61643959
1269291038269291039CT35GENIChomozygous61643960
1269291739269291740AG25GENIChomozygous61643961
1269292635269292636CT38GENIChomozygous61643962
1269294274269294275TC27GENIChomozygous61210806
1269296881269296883GC--21GENIChomozygous61643963
1269297939269297940TC20GENIChomozygous61643964
1269298098269298099GA21GENIChomozygous61643965
1269298524269298525CT24GENIChomozygous61643966
1269298751269298761ACACACACAC----------10GENICpossibly homozygous61643967
1269298753269298761ACACACAC--------10GENICheterozygous61684464
1269298813269298814CT40GENICpossibly homozygous61643968
1269298904269298905CCAT43GENIChomozygous61210832
1269299689269299690CG33GENIChomozygous61643969
1269302276269302277TA22GENIChomozygous61643970
1269304503269304504CA29GENIChomozygous61643971