chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182376654723766556CCACCCCAG4GENIChomozygous140215800
182376658123766582AT11GENIChomozygous140286752
182376701123767012GA38GENIChomozygous140286753
182376726823767269GA31GENIChomozygous140286754
182376872823768729TA43GENICpossibly homozygous140286755
182376909923769099GTGTGTAT33GENIChomozygous140215801
182376918423769185TG39GENIChomozygous140286756
182376958023769581AG39GENIChomozygous140286757
182377003423770035TG36GENIChomozygous140286758
182377097323770974CT50GENIChomozygous140286759
182377137923771380AG44GENIChomozygous140286760
182377168623771687AG40GENIChomozygous140286761
182377186823771869TG64GENICpossibly homozygous140286762
182377204423772045CT42GENIChomozygous140286763
182377241123772412CT35GENIChomozygous140286767
182377209823772099CT39GENIChomozygous140286764
182377212923772130TC40GENIChomozygous140286765
182377217623772177GA40GENICpossibly homozygous140286766
182377273223772733AG33GENIChomozygous140286768
182377337323773374GA34GENIChomozygous140286769
182377339423773395GA33GENIChomozygous140286770
182377345023773451A30GENIChomozygous140215802
182377346523773466AG33GENIChomozygous140286771
182377383223773833TC34GENIChomozygous140286772
182377409723774098AG41GENIChomozygous140286773