chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
39397084993970850GA34GENIChomozygous119981806
39397290993972910TC42GENIChomozygous111958198
39397306393973064AC35GENIChomozygous111958200
39397306993973070GA34GENIChomozygous119981808
39397325993973260AT29GENIChomozygous111958202
39397329493973295TC21GENIChomozygous112443073
39397384093973841AT28GENIChomozygous111958204
39397406193974062GT29GENIChomozygous119981810
39397537793975378TC29GENIChomozygous119981812
39397742993977430GA31GENIChomozygous111958210
39397750393977504CA35GENIChomozygous119981814
39397916093979161TG25GENIChomozygous111958212
39397934793979348GA13GENIChomozygous119981816
39397944993979450AT2GENIChomozygous120018092
39397945093979451AT3GENIChomozygous120018093
39398040993980410TC24GENIChomozygous119981818
39398142893981429TC29GENIChomozygous111958214
39398167893981679GA30GENIChomozygous119981820
39398509193985092AG44GENIChomozygous111958218
39398602993986030TA62GENIChomozygous119981822
39398604393986044CT65GENIChomozygous119981824
39398677793986778AG61GENICpossibly homozygous119981826
39398704393987044TC48GENIChomozygous111958220
39398785893987859TA12GENIChomozygous119981828
39398816093988161GA47GENIChomozygous119981830
39398840793988408TC17GENIChomozygous111958224
39398976893989769AG25GENIChomozygous119981832
39399161193991612TA34GENIChomozygous111958228
39399282793992828GA16GENIChomozygous119981834
39399295793992958GT21GENIChomozygous111958230
39399893793998938TC10GENIChomozygous111958245