chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728373617283737GA50GENIChomozygous980250080
141728481617284817CT17GENIChomozygous980250081
141728505217285053TA32GENIChomozygous980250082
141728505817285059CT34GENIChomozygous980250083
141728520317285204GC38GENIChomozygous980250084
141728587617285877CG56GENIChomozygous980250085
141728588117285882CT55GENIChomozygous980250086
141728604017286041GA16GENIChomozygous980250087
141728610817286109AC12GENIChomozygous980250088
141728669517286696CT49GENIChomozygous980250089
141728676817286769TA65GENIChomozygous980250090
141728677617286777TC61GENIChomozygous980250091
141728685817286859TC44GENIChomozygous980250092
141728703617287037CA20GENIChomozygous980250093
141728704817287049CT20GENIChomozygous980250094
141728710317287104CT16GENICpossibly homozygous980250095
141728766817287669TA8GENIChomozygous980250096
141728781917287820TG34GENIChomozygous980250097
141728792417287925CT47GENIChomozygous980250098
141728817517288176GA28GENIChomozygous980250099
141728961817289619GA32GENIChomozygous980250100
141728963217289633AG24GENIChomozygous980250101
141728977417289775GA26GENIChomozygous980250102
141728978717289788AG22GENIChomozygous980250103
141729025017290251TC40GENIChomozygous980250104
141729122717291228CA47GENIChomozygous980250105
141729125217291253TC48GENIChomozygous980250106
141729141717291418CG41GENIChomozygous980250107
141729148217291483GC37GENIChomozygous980250108
141729170017291701CT35GENIChomozygous980250109
141729201917292020CT47GENIChomozygous980250110
141729228617292287GC52GENIChomozygous980250111
141729231617292317CT56GENIChomozygous980250112
141729294717292948GT40GENIChomozygous980250113
141729295017292951CT40GENIChomozygous980250114
141729329117293292TC16GENIChomozygous980250115
141729339117293392AG36GENIChomozygous980250116
141729348817293489AG52GENIChomozygous980250117
141729502417295025TC20GENIChomozygous980250118
141729696617296967GA28GENIChomozygous980250119