chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728380217283803TG14GENIChomozygous964999756
141728481617284817CT29GENIChomozygous964999757
141728489917284900CT37GENIChomozygous964999758
141728505217285053TA25GENIChomozygous964999759
141728505817285059CT23GENIChomozygous964999760
141728520317285204GC11GENIChomozygous964999761
141728529317285294TG8GENIChomozygous964999762
141728531217285313CG6GENIChomozygous964999763
141728533317285334TC3GENIChomozygous964999764
141728563217285633CT25GENIChomozygous964999765
141728587617285877CG20GENIChomozygous964999766
141728588117285882CT20GENIChomozygous964999767
141728645617286457TC21GENIChomozygous964999768
141728669517286696CT24GENIChomozygous964999769
141728676817286769TA27GENICpossibly homozygous964999770
141728677617286777TC27GENICpossibly homozygous964999771
141728685817286859TC29GENIChomozygous964999772
141728703617287037CA10GENIChomozygous964999773
141728710317287104CT4GENIChomozygous964999774
141728766817287669TA13GENIChomozygous964999775
141729113417291135GA25GENIChomozygous964999776
141729148217291483GC31GENIChomozygous964999777
141729201917292020CT30GENIChomozygous964999778
141729228617292287GC36GENIChomozygous964999779
141729295017292951CT37GENIChomozygous964999780
141729299117292992TC42GENIChomozygous964999781
141729314017293141GA40GENIChomozygous964999782
141729327917293280AC38GENIChomozygous964999783
141729329117293292TC36GENIChomozygous964999784
141729348817293489AG22GENIChomozygous964999785
141729472117294722AG34GENIChomozygous964999786
141729490717294908AG36GENIChomozygous964999787
141729502417295025TC30GENIChomozygous964999788
141729540917295410CT23GENIChomozygous964999789
141729542117295422GA18GENIChomozygous964999790
141729591217295913TC22GENIChomozygous964999791
141729593717295938AG24GENIChomozygous964999792
141729638517296386AG22GENIChomozygous964999793
141729972117299722AG19GENIChomozygous964999794
141730108917301090TG34GENIChomozygous964999795
141730127317301274TC23GENIChomozygous964999796