chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53586585635865857AG19GENIChomozygous113741971
53586590135865902AG17GENIChomozygous113741973
53586607135866072GT19GENIChomozygous113741975
53586805135868052AG23GENIChomozygous113741977
53586901135869012TA16GENIChomozygous113741979
53586921935869220GA22GENIChomozygous113741981
53587010235870103GA8GENIChomozygous113741985
53587091735870918AG16GENIChomozygous113741989
53587126335871264GT8GENIChomozygous113741990
53587177735871778AC18GENIChomozygous113741992
53587183435871835AG21GENIChomozygous113741994
53587217235872173CT5GENIChomozygous113742000
53587226835872269GA5GENIChomozygous113742002
53587228035872281AG6GENIChomozygous113742004
53587250435872505GA10GENIChomozygous113742006
53587307935873080GA12GENIChomozygous113742008
53587315435873155CT4GENIChomozygous113742010
53587353435873535CT7GENIChomozygous113742012
53587384435873845CT14GENIChomozygous113742014
53587387135873872TC6GENICheterozygous113742016
53587388035873881TC4GENICheterozygous113742018
53587749835877499AG13GENIChomozygous113742028
53587786135877862TC23GENICpossibly homozygous113742030
53587808635878087AG5GENIChomozygous126181026
53587876235878763CT5GENIChomozygous113742032
53587894235878943GA16GENIChomozygous113742034
53587908935879090AG19GENIChomozygous113742036
53587962935879630TC34GENIChomozygous113742038
53587985035879851GA8GENIChomozygous113742040
53588017435880175CG24GENIChomozygous113742042
53588044635880447CT19GENIChomozygous113742044
53588049335880494AG23GENIChomozygous113742046
53588270935882710AG23GENIChomozygous113742048
53588327435883275AG12GENIChomozygous113742050
53588332835883329AG20GENIChomozygous113742052