chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101288104412881045AC21GENICpossibly homozygous510550153
101288222312882224GA70GENIChomozygous507546838
101288263112882635ATAT----39GENIChomozygous686083529
101288342812883432AAAC----10GENIChomozygous686083530
101288555912885560GT59GENIChomozygous507546839
101288586912885870TC60GENIChomozygous507546840
101288604912886050GA42GENIChomozygous510550154
101288620912886210TG52GENIChomozygous507546841
101288653012886531GA34GENICpossibly homozygous507546842
101288653112886532GA35GENICpossibly homozygous507546843
101288655912886560GA36GENICpossibly homozygous507546844
101288659012886591CG30GENIChomozygous507546845
101288682512886826AG53GENIChomozygous507546846
101288705512887056GA67GENIChomozygous507546847
101288770912887710CT52GENIChomozygous507546848
101288821012888211TTACAC11GENIChomozygous686083531
101288929412889295AC66GENIChomozygous507546849
101288966612889667GC52GENIChomozygous507546850
101288993512889936CG64GENIChomozygous507546851
101288995712889958TC69GENIChomozygous507546852
101289005012890051AG53GENIChomozygous507546853
101289109612891097TC49GENIChomozygous507546854