chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170423607170423608CG18GENIChomozygous108958821
1170424009170424010CT27GENIChomozygous108376018
1170424784170424785CT30GENIChomozygous108376020
1170424916170424917AC18GENIChomozygous108376022
1170425360170425361GA18GENIChomozygous108376024
1170426600170426601AG39GENIChomozygous108376030
1170429010170429011CG24GENIChomozygous108376040
1170429203170429204TG28GENIChomozygous108958823
1170429262170429263AG20GENIChomozygous109166673
1170429419170429420CT13GENIChomozygous108958824
1170429519170429520AT20GENIChomozygous108958825
1170429757170429758CT27GENIChomozygous108958826
1170430150170430151AG17GENIChomozygous108958828
1170431046170431047AG18GENIChomozygous108958829