chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137937842279378422T26GENICpossibly homozygous131920878
137937856479378565C12GENIChomozygous129077286
137938176779381768AG17GENIChomozygous114402857
137938064879380649GA14GENIChomozygous114402853
137938109379381094GA16GENIChomozygous114402855
137938286279382863TC15GENIChomozygous114402859
137938539179385391A18GENICpossibly homozygous131920879
137938698479386985AG23GENIChomozygous114402863
137938791679387917AG17GENIChomozygous114402865
137938817179388172CA20GENIChomozygous114402867