chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1244598454244598455CT66GENIChomozygous135853855
1244599282244599283TG51GENIChomozygous135853856
1244601989244601990A46GENIChomozygous142797924
1244602444244602445AG55GENIChomozygous135853858
1244602532244602533TC59GENIChomozygous135853859
1244605011244605012TC46GENIChomozygous135853862
1244606120244606122TC28GENICpossibly homozygous142797925
1244611970244611970A35GENIChomozygous142797926
1244613722244613728CTCTCT46GENIChomozygous142797927
1244616355244616356TG44GENIChomozygous135853867
1244619481244619482AG61GENIChomozygous135853868
1244624702244624703GA45GENIChomozygous142879796
1244616430244616431TA52GENICheterozygous153911678
1244605632244605633GA39GENIChomozygous142879790
1244608421244608422TA52GENIChomozygous142879791
1244615317244615318GA51GENIChomozygous142879792
1244615886244615887GC55GENIChomozygous142879793
1244617551244617552GT28GENIChomozygous142879794
1244620698244620699CT40GENIChomozygous142879795
1244616430244616431T52GENICheterozygous403879906
1244625182244625183T40GENICpossibly homozygous135470504
1244625726244625727TG41GENIChomozygous135853874
1244628860244628861TC26GENIChomozygous135853881
1244630321244630322TA19GENICheterozygous402983886
1244630317244630318T19GENIChomozygous402983883
1244630317244630318TA19GENICheterozygous402983884
1244630321244630322T19GENIChomozygous402983885
1244630325244630326T19GENIChomozygous402983887
1244630325244630326TA19GENICheterozygous402983888
1244630329244630330T19GENICheterozygous402983889
1244630329244630330TA19GENIChomozygous402983890
1244630333244630334T19GENICheterozygous403549046
1244630333244630334TA19GENIChomozygous403549047
1244630338244630339TC19GENIChomozygous142879797
1244630757244630758AG47GENIChomozygous135853882
1244631462244631463TC46GENIChomozygous142879798
1244631515244631516AG51GENIChomozygous142879799
1244632773244632774GT46GENICpossibly homozygous142879800