chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728373617283737GA31GENIChomozygous970786699
141728481617284817CT35GENIChomozygous970786700
141728505217285053TA28GENIChomozygous970786701
141728505817285059CT29GENIChomozygous970786702
141728520317285204GC26GENIChomozygous970786703
141728587617285877CG25GENIChomozygous970786704
141728588117285882CT25GENIChomozygous970786705
141728604017286041GA25GENIChomozygous970786706
141728610817286109AC23GENIChomozygous970786707
141728669517286696CT55GENIChomozygous970786708
141728676817286769TA40GENIChomozygous970786709
141728677617286777TC37GENIChomozygous970786710
141728685817286859TC36GENIChomozygous970786711
141728703617287037CA16GENIChomozygous970786712
141728704817287049CT17GENIChomozygous970786713
141728710317287104CT11GENIChomozygous970786714
141728751117287512TC25GENIChomozygous970786715
141728766817287669TA10GENIChomozygous970786716
141728781917287820TG30GENIChomozygous970786717
141728792417287925CT35GENIChomozygous970786718
141728817517288176GA21GENIChomozygous970786719
141728961817289619GA15GENIChomozygous970786720
141728963217289633AG18GENIChomozygous970786721
141728977417289775GA35GENIChomozygous970786722
141728978717289788AG31GENIChomozygous970786723
141729025017290251TC31GENIChomozygous970786724
141729122717291228CA32GENIChomozygous970786725
141729125217291253TC33GENIChomozygous970786726
141729141717291418CG28GENIChomozygous970786727
141729148217291483GC28GENIChomozygous970786728
141729170017291701CT29GENIChomozygous970786729
141729201917292020CT24GENIChomozygous970786730
141729228617292287GC50GENIChomozygous970786731
141729231617292317CT45GENIChomozygous970786732
141729329117293292TC25GENIChomozygous970786733
141729339117293392AG27GENIChomozygous970786734
141729348817293489AG39GENIChomozygous970786735
141729502417295025TC23GENIChomozygous970786736
141729696617296967GA36GENIChomozygous970786737