chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204128233841282339CA25GENIChomozygous109196113
204128305341283054AT18GENIChomozygous109196125
204128324541283246GC10GENIChomozygous109196127
204128344341283444CA9GENIChomozygous109401571
204128390941283910GA10GENIChomozygous109268065
204128522141285222GT10GENIChomozygous109461982
204128550141285502AC14GENIChomozygous119795255
204128929141289292CA9GENIChomozygous109459091
204128933941289340GC15GENIChomozygous109196131
204129350141293502TA17GENICpossibly homozygous109531004
204129351341293514GT7GENIChomozygous109268081
204129351541293516CT8GENIChomozygous109268083
204129354041293541AT15GENIChomozygous109268087
204129358441293585GT12GENIChomozygous109196136
204129359041293591CG13GENIChomozygous109531008
204129360641293607GA12GENIChomozygous109531010
204129364741293648GT7GENIChomozygous109401575
204135752641357527TC4GENIChomozygous109315874
204136236841362369AG8GENIChomozygous109531022