chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728481617284817CT20GENIChomozygous976955036
141728505217285053TA20GENIChomozygous976955037
141728505817285059CT20GENIChomozygous976955038
141728520317285204GC17GENIChomozygous976955039
141728587617285877CG10GENIChomozygous976955040
141728588117285882CT13GENIChomozygous976955041
141728604017286041GA14GENIChomozygous976955042
141728610817286109AC11GENIChomozygous976955043
141728669517286696CT14GENICpossibly homozygous976955044
141728676817286769TA13GENIChomozygous976955045
141728685817286859TC7GENIChomozygous976955046
141728703617287037CA4GENIChomozygous976955047
141728704817287049CT3GENIChomozygous976955048
141728781917287820TG24GENIChomozygous976955049
141728792417287925CT16GENIChomozygous976955050
141728817517288176GA33GENIChomozygous976955051
141728961817289619GA28GENIChomozygous976955052
141728963217289633AG27GENIChomozygous976955053
141728977417289775GA15GENIChomozygous976955054
141728978717289788AG14GENIChomozygous976955055
141729025017290251TC7GENIChomozygous976955056
141729108717291088CT10GENIChomozygous976955057
141729122717291228CA17GENIChomozygous976955058
141729125217291253TC20GENIChomozygous976955059
141729148217291483GC20GENIChomozygous976955060
141729201917292020CT17GENIChomozygous976955061
141729228617292287GC26GENIChomozygous976955062
141729231617292317CT30GENIChomozygous976955063
141729294717292948GT16GENIChomozygous976955064
141729295017292951CT16GENIChomozygous976955065
141729329117293292TC22GENIChomozygous976955066
141729339117293392AG15GENIChomozygous976955067
141729348817293489AG11GENIChomozygous976955068
141729502417295025TC30GENIChomozygous976955069
141729696617296967GA23GENIChomozygous976955070