chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64648571146485712TG22GENIChomozygous606791856
64648590746485908AT22GENIChomozygous606791857
64648611546486116TTC19GENIChomozygous733340953
64648654346486544GC22GENIChomozygous606791858
64648729846487299CT30GENIChomozygous606791859
64648740146487402CT30GENIChomozygous606791860
64648770946487710CCT16GENICpossibly homozygous733340955
64648778746487788AG13GENIChomozygous606791861
64648785446487855G-17GENIChomozygous733340956
64648813746488138AACGCG17GENICpossibly homozygous733340957
64648814246488143CT15GENICpossibly homozygous609007255
64648834346488344C-1GENIChomozygous733340958
64648858946488590AG29GENIChomozygous606791862
64648864946488650CG31GENIChomozygous606791863
64648870146488702TC31GENIChomozygous609007256
64648894846488949GA16GENIChomozygous606791864
64648910046489101GC15GENIChomozygous606791865
64648971946489720CT22GENIChomozygous606791866
64648975046489751CG27GENIChomozygous606791867
64648980046489801AG26GENIChomozygous606791868
64648981546489816CT24GENIChomozygous606791869
64648990546489906G-14GENIChomozygous733340959
64648992646489927CT16GENIChomozygous606791870