chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2051087025108703TC26GENIChomozygous109076889
2051090555109056AC32GENIChomozygous109076891
2051091195109120CT25GENIChomozygous109076893
2051092445109245T21GENIChomozygous129653142
2051093105109311GC23GENIChomozygous109076895
2051095665109567AG26GENIChomozygous109076897
2051096605109661AG24GENIChomozygous109076899
2051097055109706TG16GENIChomozygous109076901
2051097265109727TG17GENIChomozygous109076903
2051097585109759AG22GENIChomozygous109076905
2051101965110197AG16GENIChomozygous109076907
2051106955110696TA14GENIChomozygous109076909
2051108955110896GA18GENIChomozygous109076911
2051109455110946CT23GENIChomozygous109076913
2051110065111007TC21GENIChomozygous109076915
2051111735111174CT30GENIChomozygous109076917
2051112625111263CT24GENIChomozygous109076919
2051113165111317C17GENIChomozygous130186143
2051113215111322C17GENIChomozygous130186144
2051113275111327AA18GENIChomozygous129653143
2051114535111454CT23GENIChomozygous109076921
2051116905111691AT24GENIChomozygous109076923
2051120505112051C15GENIChomozygous129653144
2051120855112086TC15GENIChomozygous109076925
2051123055112306TC14GENIChomozygous109076927
2051124125112413C21GENIChomozygous129653145
2051124725112473AG15GENIChomozygous109076929
2051124985112499GA15GENIChomozygous109076931
2051126075112608AG17GENIChomozygous109076933
2051126375112638TC18GENIChomozygous109076935
2051126855112686G12GENIChomozygous129653146
2051128245112825GC13GENIChomozygous109076937
2051128305112832GG13GENIChomozygous129653147
2051129275112928AG17GENIChomozygous109233840
2051129385112939CG19GENIChomozygous109076939
2051130275113028TC21GENIChomozygous109076941
2051132615113262GA22GENIChomozygous109076943
2051133495113350CT11GENIChomozygous109076945