chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12119826321198264GA41GENIChomozygous142822926
12119850921198510A27GENICpossibly homozygous402942038
12119850921198510AC27GENICheterozygous402942039
12119906421199065AG53GENIChomozygous142822927
12119948121199482GA51GENIChomozygous142822928
12120102521201026TC52GENIChomozygous142822929
12120341921203420AG40GENIChomozygous142822930
12120627621206277GA42GENIChomozygous142822931
12121342421213425C27GENICheterozygous402942043
12121342421213425CG27GENICheterozygous402942044
12121348621213487CG29GENICheterozygous402942045
12121348621213487C29GENICheterozygous402942046
12121349621213497CG31GENICheterozygous402942051
12121349621213497C31GENICheterozygous402942052
12121855721218558GT58GENIChomozygous142822932
12121046821210469A43GENIChomozygous142786321
12120833921208339G6GENIChomozygous142786320