chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4026826940268270GT1GENIChomozygous130198766
X4027486240274863AG12GENICheterozygous120791782
X4027489540274896GA10GENICheterozygous130805941
X4029230340292304GA16GENIChomozygous108256724
X4027515340275153CTGA9GENIChomozygous129737466
X4027566740275667A13GENIChomozygous129737467
X4027893840278938TG8GENIChomozygous129737468
X4028138140281381T12GENIChomozygous129737469
X4029029340290294TG12GENIChomozygous108446450
X4029227940292280TC15GENIChomozygous108256716
X4029228040292281AT16GENIChomozygous108256718
X4029228240292283AC16GENIChomozygous108256720
X4029230240292303AT16GENIChomozygous108256722
X4029230740292308CG15GENIChomozygous108256726
X4029235440292355TG10GENIChomozygous108256728
X4029236040292361GC8GENIChomozygous108256730
X4029245540292456C12GENIChomozygous129737470
X4029247340292474AG12GENIChomozygous108256732
X4030465140304652AC7GENIChomozygous119917033
X4030483340304833T13GENIChomozygous129737472