chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1244598454244598455CT23GENIChomozygous135853855
1244599282244599283TG19GENIChomozygous135853856
1244601107244601108TC18GENIChomozygous145339677
1244602444244602445AG16GENIChomozygous135853858
1244602532244602533TC21GENIChomozygous135853859
1244605011244605012TC26GENIChomozygous135853862
1244606120244606122TC25GENICpossibly homozygous142797925
1244611970244611970A22GENIChomozygous142797926
1244613722244613728CTCTCT21GENIChomozygous142797927
1244608421244608422TA24GENIChomozygous142879791
1244611597244611598GA23GENIChomozygous145339678
1244616355244616356TG17GENIChomozygous135853867
1244619481244619482AG24GENIChomozygous135853868
1244620698244620699CT18GENIChomozygous142879795
1244624899244624900TA30GENIChomozygous145339679
1244625182244625183T17GENIChomozygous135470504
1244625726244625727TG26GENIChomozygous135853874
1244626654244626654CT17GENIChomozygous145250435
1244628860244628861TC16GENIChomozygous135853881
1244629735244629736CG23GENIChomozygous145339680
1244630329244630330TA14GENIChomozygous402983890
1244616430244616431TA21GENIChomozygous153911678
1244616430244616431T21GENICheterozygous403879906
1244630317244630318T14GENIChomozygous402983883
1244630317244630318TA14GENICheterozygous402983884
1244630321244630322T14GENIChomozygous402983885
1244630321244630322TA14GENICheterozygous402983886
1244630325244630326T14GENIChomozygous402983887
1244630325244630326TA14GENICheterozygous402983888
1244630329244630330T14GENICheterozygous402983889
1244630338244630339TC14GENIChomozygous142879797
1244630757244630758AG26GENIChomozygous135853882
1244630333244630334T14GENICheterozygous403549046
1244630333244630334TA14GENIChomozygous403549047
1244630850244630851GC19GENIChomozygous148671398