chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170423607170423608CG16GENIChomozygous108958821
1170424009170424010CT25GENIChomozygous108376018
1170424784170424785CT26GENIChomozygous108376020
1170424916170424917AC13GENIChomozygous108376022
1170425360170425361GA7GENIChomozygous108376024
1170425803170425804GC5GENICheterozygous109052136
1170426600170426601AG27GENIChomozygous108376030
1170429010170429011CG15GENIChomozygous108376040
1170429203170429204TG27GENIChomozygous108958823
1170429419170429420CT18GENIChomozygous108958824
1170429757170429758CT18GENIChomozygous108958826
1170430150170430151AG16GENICheterozygous108958828
1170431046170431047AG24GENIChomozygous108958829
1170429262170429263AG20GENIChomozygous109166673