chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15353167253531673TC25GENICpossibly homozygous108098109
15353215753532158AG25GENICpossibly homozygous108098110
15353219553532196CA31GENICpossibly homozygous108098111
15353248453532485CA34GENICpossibly homozygous108098112
15353367553533676GA24GENIChomozygous108098116
15353374353533744TC15GENIChomozygous108098117
15353375253533753AC17GENIChomozygous108098118
15353557053535571AG21GENICpossibly homozygous108098121
15353572753535728AC28GENICpossibly homozygous108098122
15353581353535814CT23GENIChomozygous108098123
15353659953536600TG33GENICpossibly homozygous108098124
15353693253536933GA14GENIChomozygous108098125
15353693353536934TG14GENIChomozygous120521851
15353726053537261AG16GENIChomozygous108098126
15353731753537318TC31GENICpossibly homozygous108098127
15353741853537419AC19GENIChomozygous108098128
15353849053538491AG15GENIChomozygous108098129
15353865953538660AG28GENICpossibly homozygous108098130
15354248153542482CT34GENIChomozygous108098134
15354473053544731AC33GENICpossibly homozygous108098135
15354529953545300TC21GENIChomozygous108098136
15354648153546482TA30GENICpossibly homozygous108098138
15354738753547388CG21GENIChomozygous108098139
15354739153547392TC24GENIChomozygous108098140
15354828753548288GT21GENIChomozygous108098141
15354837653548377CG22GENIChomozygous108098142
15354850653548507TC31GENICpossibly homozygous108098143
15354863353548634GA29GENICpossibly homozygous108098144
15354865453548655CT35GENICpossibly homozygous108098145
15354871353548714CT39GENICpossibly homozygous108098146
15354875153548752GT34GENIChomozygous108098147
15354876453548765GA32GENICpossibly homozygous108098148
15354944153549442TC37GENIChomozygous108098149
15355115253551153TC29GENIChomozygous108098153
15355332153553322GA28GENIChomozygous108098154