chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22514717125147172AG23GENIChomozygous110491152
22514730125147302CT20GENIChomozygous110491156
22514743125147432AG17GENIChomozygous110491158
22514743225147433TC17GENIChomozygous110491160
22514747825147479TA21GENIChomozygous120141086
22514804125148042CT18GENIChomozygous110675635
22514810325148104AG17GENIChomozygous110675637
22514821725148218GA15GENIChomozygous110675639
22514859825148599AG18GENIChomozygous110927581
22514890825148909AG26GENIChomozygous110675641
22514899625148997CT25GENIChomozygous110675647
22514902425149025GA27GENIChomozygous110927582
22514905125149052AG23GENIChomozygous110927583
22514912425149125CG24GENIChomozygous110675649
22514944725149448CT21GENIChomozygous110927584
22514955525149556TC16GENIChomozygous109649525
22514957525149576GA16GENIChomozygous110927585
22514961325149614CT20GENIChomozygous110927586
22514994025149941GA13GENIChomozygous110927587
22515037525150376CT25GENIChomozygous110927588
22515041125150412CT25GENIChomozygous110927589
22515047825150479GA28GENIChomozygous109649529
22515054025150541CT25GENIChomozygous109649531
22515076425150765CT17GENIChomozygous110927590
22515100425151005GA10GENIChomozygous110927591
22515119325151194TG18GENIChomozygous110675661
22515124025151241AG18GENIChomozygous110927592
22515157925151580TG12GENIChomozygous110927594
22515177425151775AC12GENIChomozygous110675663
22515228325152284AT15GENIChomozygous110927595
22515265625152657TC16GENIChomozygous110927596
22515310125153102AG29GENIChomozygous109649533
22515324825153249GA21GENIChomozygous110927597