chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5164038606164038607T-10GENICheterozygous55828092
5164041448164041449GA36GENIChomozygous55944286
5164041643164041644TC24GENIChomozygous55944287
5164041650164041651AG18GENIChomozygous55944289
5164042058164042059AG29GENIChomozygous55944291
5164042530164042534ACAC----7GENIChomozygous55944293
5164047193164047194AT25GENIChomozygous55944295
5164050648164050649TC31GENIChomozygous55944299
5164053931164053932AG24GENIChomozygous55828113
5164054989164054999GAGCCGAGCC----------8GENICpossibly homozygous55828116
5164057199164057200AG34GENIChomozygous55828120
5164057329164057330AG23GENIChomozygous55828121
5164058262164058263TC29GENIChomozygous55828123
5164058723164058724CCT25GENICpossibly homozygous55944303
5164061613164061614AG30GENIChomozygous55828124
5164062570164062571CA36GENIChomozygous55944305
5164062972164062973A-23GENICpossibly homozygous55828126
5164063260164063275ATCATCATCATCATC---------------8GENIChomozygous56464158
5164063372164063373GA41GENIChomozygous55944309
5164063677164063678CCGGGGG4GENICheterozygous56555079
5164064186164064187TC12GENIChomozygous55828128