chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121970420619704207TG22GENIChomozygous884222049
121970467219704673TA5GENIChomozygous884222050
121970487919704880GT7GENICheterozygous884222051
121970490519704906TC20GENICheterozygous884222052
121970492119704922GA15GENICheterozygous884222053
121970494419704945AT14GENIChomozygous884222054
121970511919705120GT16GENIChomozygous884222055
121970514919705150AG9GENIChomozygous884222056
121970577919705780GA4GENIChomozygous884222057
121970595119705952TC15GENIChomozygous884222058
121970602219706023CT14GENIChomozygous884222059
121970650619706507AT15GENIChomozygous884222060
121970703219707033CT12GENICheterozygous884222061
121970703319707034GT13GENICheterozygous884222062
121970704519707046CT20GENICheterozygous884222063
121970717919707180AC13GENIChomozygous884222064
121970745819707459AG10GENIChomozygous884222065
121970751619707517GA14GENIChomozygous884222066
121970754019707541AT14GENIChomozygous884222067
121970756519707566CG15GENIChomozygous884222068
121970801019708011CT18GENIChomozygous884222069
121970804819708049CA12GENIChomozygous884222070