chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74160145041601451GA17GENIChomozygous53890861
74160148941601490CT23GENIChomozygous53890862
74160182941601830AATT20GENIChomozygous53890863
74160196541601966CT28GENIChomozygous53890864
74160227841602279CT19GENIChomozygous53890865
74160228741602288GA19GENIChomozygous53890866
74160233441602335TC14GENIChomozygous53890867
74160374841603749TC16GENIChomozygous53890868
74160461641604617CT9GENIChomozygous53890869
74160475041604751AG11GENIChomozygous53890870
74160486041604861TTG7GENIChomozygous53890871
74160500841605009GA7GENIChomozygous53890872
74160526341605264GA17GENIChomozygous53890876
74160554441605545C-16GENIChomozygous53890877
74160578641605787TG22GENIChomozygous53890878
74160609141606092GGACAT12GENIChomozygous53890879
74160666941606670TC19GENIChomozygous53890880
74160745741607458TTA15GENIChomozygous53890882
74160778341607784GA14GENIChomozygous53890884
74161008541610086CT8GENIChomozygous53890895
74161067941610682GGG---7GENIChomozygous53890896
74161211041612111TC17GENIChomozygous53890900
74161254641612547GA17GENIChomozygous54366190
74161064441610645CA15GENIChomozygous54366184
74161141741611418AT9GENIChomozygous54366186
74161244241612443GC14GENIChomozygous54366188
74161259241612593GT24GENIChomozygous54366192
74161266941612670T-19GENIChomozygous54366194
74161274141612742TTA14GENICpossibly homozygous53890903
74161295241612953T-20GENIChomozygous53890907
74161317941613180GA17GENIChomozygous53890909
74161349241613493GA13GENIChomozygous53890910
74161368641613687AG12GENIChomozygous53890911
74161385841613859TC14GENIChomozygous53890913
74161402741614028GA17GENIChomozygous54366198
74161472641614727A-16GENIChomozygous53890915
74161486641614867GC11GENIChomozygous54366200
74161515841615159GC16GENIChomozygous54366202