chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1534733573473361GTGT----2GENIChomozygous49025719
1534900713490072AT23GENIChomozygous48223873
1534978213497822A-4GENICheterozygous49184642
1535019043501905TTATA5GENIChomozygous48223875
1535091243509125A-6GENIChomozygous48223876
1535091303509131AAG5GENIChomozygous48223877
1535091393509140AG4GENIChomozygous49079028
1535091413509142TA4GENIChomozygous49079030
1535121793512209ATGATTTCTGTTTAAATATCCTAGCATTGA------------------------------24GENICheterozygous49079035
1535122123512216CAAT----7GENICheterozygous49079037
1535122193512222CAA---9GENICheterozygous49079039
1535161223516123GC4GENIChomozygous48223880
1535163243516325C-19GENIChomozygous48223881
1535177343517736CA--9GENICheterozygous49237560
1535210083521010TC--7GENICheterozygous49243136
1535221813522182AC29GENIChomozygous48223882
1535221823522183CA30GENIChomozygous48451909
1535233443523345CCA8INTERGENICheterozygous48451912
1535247533524754TG27INTERGENIChomozygous48451914
1535247553524756GT27INTERGENIChomozygous48451916
1535339723533973CG30INTERGENIChomozygous48223883
1535339883533989TG33INTERGENIChomozygous48944578
1535339893533990GT33INTERGENIChomozygous48944581
1535440823544083C-21INTERGENIChomozygous48223885
1535441783544179CA33INTERGENICpossibly homozygous48223886