chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8119787209119787210GA12GENIChomozygous138434755
8119787210119787211AG12GENIChomozygous138434756
8119788041119788042CT13GENIChomozygous138434757
8119788604119788605CT12GENIChomozygous142105758
8119788796119788797GA18GENIChomozygous138434758
8119789388119789389TC18GENIChomozygous138434759
8119789719119789720TC16GENIChomozygous138434760
8119789916119789917CT15GENIChomozygous138434761
8119790149119790150GA10GENIChomozygous138434762
8119790324119790325CT16GENIChomozygous138434763
8119790402119790403AG12GENIChomozygous138434764
8119790769119790770AG17GENIChomozygous138434765
8119790809119790810CA17GENIChomozygous138434766
8119790924119790925AG20GENIChomozygous138434767
8119792262119792263CT12GENIChomozygous142105759
8119792647119792648CT13GENIChomozygous138434768
8119792762119792763CG8GENIChomozygous138434769
8119792887119792888CG9GENIChomozygous138434770
8119793158119793159GC15GENIChomozygous138434771
8119793212119793213TC14GENIChomozygous138434772
8119793949119793950TG19GENIChomozygous138434773
8119794256119794257GA8GENIChomozygous138434774
8119794890119794891AT18GENIChomozygous138434775
8119795773119795774AC20GENIChomozygous138434776
8119795821119795821CCTCTAGTACAGTACTCCTCTAGTACAGTACC17GENIChomozygous138269142
8119794788119794792ACAC12GENIChomozygous138269141
8119792695119792701CCCTCT9GENIChomozygous138269139
8119794420119794421A19GENIChomozygous138269140
8119796340119796341GT20GENIChomozygous138434777
8119796930119796931CT28GENIChomozygous142105760
8119797148119797149CA16GENIChomozygous138434778
8119797744119797745TA15GENIChomozygous138434779
8119798927119798928AT13GENIChomozygous138434782
8119798338119798339GA14GENIChomozygous138434780
8119798648119798649GA13GENIChomozygous138434781