chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121970408619704087TA12GENIChomozygous874770545
121970420619704207TG21GENIChomozygous874770546
121970487919704880GT6GENICheterozygous874770547
121970490519704906TC18GENICheterozygous874770548
121970494419704945AT18GENIChomozygous874770549
121970511919705120GT11GENIChomozygous874770550
121970514919705150AG7GENIChomozygous874770551
121970595119705952TC17GENIChomozygous874770552
121970602219706023CT12GENIChomozygous874770553
121970611019706111CT14GENICheterozygous874770554
121970650619706507AT18GENIChomozygous874770555
121970703219707033CT12GENICheterozygous874770556
121970704519707046CT9GENICheterozygous874770557
121970717919707180AC7GENIChomozygous874770558
121970745819707459AG7GENIChomozygous874770559
121970751619707517GA16GENIChomozygous874770560
121970754019707541AT13GENIChomozygous874770561
121970756519707566CG16GENIChomozygous874770562
121970801019708011CT20GENIChomozygous874770563
121970804819708049CA12GENIChomozygous874770564