chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121970420619704207TG14GENIChomozygous881087111
121970467219704673TA4GENIChomozygous881087112
121970490519704906TC20GENICheterozygous881087113
121970492119704922GA12GENICheterozygous881087114
121970494419704945AT17GENIChomozygous881087115
121970511919705120GT17GENIChomozygous881087116
121970514919705150AG5GENIChomozygous881087117
121970530619705307TA4GENICheterozygous881087118
121970530719705308GC4GENICheterozygous881087119
121970577919705780GA7GENIChomozygous881087120
121970595119705952TC24GENIChomozygous881087121
121970602219706023CT13GENIChomozygous881087122
121970611019706111CT17GENICheterozygous881087123
121970650619706507AT15GENIChomozygous881087124
121970703219707033CT11GENICheterozygous881087125
121970704519707046CT10GENICheterozygous881087126
121970717919707180AC11GENIChomozygous881087127
121970740819707409AC4GENIChomozygous881087128
121970745819707459AG11GENIChomozygous881087129
121970751619707517GA14GENIChomozygous881087130
121970754019707541AT16GENIChomozygous881087131
121970756519707566CG20GENIChomozygous881087132
121970801019708011CT24GENIChomozygous881087133
121970804819708049CA15GENIChomozygous881087134