chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13149405131494052CA17GENIChomozygous108713959
13149409031494091CA5GENIChomozygous108713961
13149492031494921TC17GENIChomozygous108713963
13149497031494971TC16GENIChomozygous108713965
13149498131494982AT16GENIChomozygous108713967
13149505831495059AG17GENIChomozygous108713969
13149515031495151AT25GENIChomozygous108713971
13149519631495197CA13GENIChomozygous108713973
13149562431495625CT11GENIChomozygous108713979
13149576831495769GA13GENIChomozygous108713981
13149650531496506CG17GENIChomozygous108713985
13149668731496688GA15GENIChomozygous108713987
13149670531496706CT12GENIChomozygous108713989
13149688831496889GA17GENIChomozygous108713991
13149700131497002TC14GENIChomozygous108713993
13149711231497113AC19GENIChomozygous108713995
13149763331497634TA14GENIChomozygous108713997
13149808831498089AG24GENIChomozygous108714001
13149826931498270TC11GENIChomozygous108714003
13149902631499027TC12GENIChomozygous108714007
13149954731499548TC21GENIChomozygous109072128
13149970231499703AC19GENIChomozygous108714009
13149977631499777GA16GENIChomozygous108714011
13150075131500752AC10GENIChomozygous109072130
13150082731500828TC10GENIChomozygous108714017
13150126831501269CT4GENIChomozygous108714051
13150525831505259GA20GENIChomozygous108714091
13150537531505376CA29GENIChomozygous108714095
13150620931506210CT13GENIChomozygous109072148
13150625831506259CT21GENIChomozygous109072150
13151108731511088TC18GENIChomozygous108714125
13151109831511099AG16GENIChomozygous108714127
13151242831512429GA4GENIChomozygous108714137
13151251831512519AG9GENIChomozygous108714139
13151501931515020AC13GENIChomozygous109072154
13151757731517578AG18GENIChomozygous108714251