chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98181891981818920AG23GENIChomozygous117586516
98181941581819416TC42GENIChomozygous117586518
98182038181820382GA27GENIChomozygous120418739
98182038281820383CT27GENIChomozygous117849141
98182152681821527TG25GENIChomozygous117586532
98182281581822816TC42GENIChomozygous117849142
98182866081828661TC42GENIChomozygous117849143
98182867081828671AG50GENIChomozygous120418740
98182867581828676TA50GENIChomozygous120418741
98182971181829712CA7GENIChomozygous117849144
98182984181829842GA22GENIChomozygous117586588
98183022881830229GA69GENIChomozygous117849145
98183026681830267GA59GENICpossibly homozygous117849146
98183032181830322GA46GENIChomozygous117849147
98183081581830816AT12GENIChomozygous117849148
98183097281830973TA37GENIChomozygous117849149
98183597581835976GA50GENIChomozygous117849150
98183598881835989AT50GENIChomozygous117849151
98183613881836139TC45GENIChomozygous117586592
98183620181836202TC42GENIChomozygous120279555
98183622281836223TC44GENIChomozygous117586594
98183638881836389GA36GENIChomozygous117849152
98183959981839600AG40GENIChomozygous117586600
98184039581840396AG37GENIChomozygous117849153
98184102881841029TG12GENIChomozygous117849154
98184103981841040TG12GENIChomozygous117849155
98184135481841355TA17GENIChomozygous120418742
98184230681842307CT19GENIChomozygous117849156
98184294381842944GA16GENIChomozygous117586604
98184347581843476TC39GENIChomozygous117849157
98184354681843547TC31GENIChomozygous117586606
98184371081843711CT33GENIChomozygous117586608
98184428781844288AT51GENIChomozygous117849158
98182685481826855AG25GENIChomozygous117380979