chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121970408619704087TA6GENIChomozygous887382088
121970420619704207TG14GENIChomozygous887382089
121970490519704906TC17GENICheterozygous887382090
121970494419704945AT17GENIChomozygous887382091
121970511919705120GT17GENIChomozygous887382092
121970514919705150AG8GENIChomozygous887382093
121970570919705710CA7GENICheterozygous887382094
121970595119705952TC14GENIChomozygous887382095
121970602219706023CT9GENIChomozygous887382096
121970650619706507AT21GENIChomozygous887382097
121970703319707034GT6GENIChomozygous887382098
121970704519707046CT6GENIChomozygous887382099
121970717919707180AC5GENIChomozygous887382100
121970733619707337GT4GENICheterozygous887382101
121970743519707436TC12GENIChomozygous887382102
121970745819707459AG9GENIChomozygous887382103
121970751619707517GA13GENIChomozygous887382104
121970754019707541AT11GENIChomozygous887382105
121970756519707566CG16GENIChomozygous887382106
121970801019708011CT20GENIChomozygous887382107
121970804819708049CA18GENIChomozygous887382108