chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121970420619704207TG10GENIChomozygous878031842
121970467219704673TA10GENIChomozygous878031843
121970490519704906TC25GENICheterozygous878031844
121970494419704945AT22GENIChomozygous878031845
121970511919705120GT17GENIChomozygous878031846
121970514919705150AG12GENIChomozygous878031847
121970530619705307TA3GENICheterozygous878031848
121970530719705308GC3GENICheterozygous878031849
121970595119705952TC15GENIChomozygous878031850
121970602219706023CT9GENIChomozygous878031851
121970650619706507AT16GENIChomozygous878031852
121970703219707033CT6GENICheterozygous878031853
121970703319707034GT4GENICheterozygous878031854
121970704519707046CT9GENICheterozygous878031855
121970717919707180AC10GENIChomozygous878031856
121970745819707459AG6GENIChomozygous878031857
121970751619707517GA17GENIChomozygous878031858
121970754019707541AT17GENIChomozygous878031859
121970756519707566CG16GENIChomozygous878031860
121970801019708011CT18GENIChomozygous878031861
121970804819708049CA11GENIChomozygous878031862