chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144292867442928675AC61GENIChomozygous66292716
144292961742929618CG33GENIChomozygous66292719
144292962142929622CG32GENICpossibly homozygous66292722
144292992142929922TA30GENIChomozygous66292725
144293037642930377TG42GENICheterozygous65943645
144293038742930388GT34GENICheterozygous66414554
144293050842930509GA57GENICheterozygous66292728
144293053242930533AG51GENICpossibly homozygous65943647
144293059042930591AG33GENICheterozygous66292731
144293059242930593GA30GENICheterozygous66292734
144293192942931930GA10GENIChomozygous66292737
144293200842932009GC20GENIChomozygous66292740
144293307442933075CT18GENICpossibly homozygous66292743
144293429242934293AG18GENIChomozygous66292746
144293431542934316AG26GENIChomozygous66292749
144293453142934532CT38GENIChomozygous66292752
144293453542934536TC37GENIChomozygous66292755
144293530042935301CT22GENIChomozygous66292758
144293539042935391CT25GENIChomozygous66292761
144293552242935523TA26GENIChomozygous66292764
144293615642936157TA28GENICheterozygous66292767
144293648042936481GA30GENIChomozygous66292770
144293652442936525CA38GENIChomozygous66292773
144293656142936562GA71GENIChomozygous66292776
144293657442936575TC72GENIChomozygous66292779
144293725842937259GT30GENICheterozygous66414555
144293731642937317AT20GENIChomozygous66292782
144293732342937324TC18GENIChomozygous66292785
144293748442937485CT16GENIChomozygous66292788
144293801242938013GA29GENICpossibly homozygous66292791
144293806042938061CT52GENICpossibly homozygous66292794
144293814942938150CT21GENIChomozygous66292797
144293838942938390TA36GENIChomozygous66292800
144293851842938519GA28GENIChomozygous66292803
144293857342938574AG29GENIChomozygous66292806
144293857642938577GC29GENIChomozygous66292809
144293858942938590CG36GENIChomozygous66292812
144293862842938629TA43GENIChomozygous66292815
144293883742938838CT28GENIChomozygous66292818
144293888042938881AT24GENIChomozygous66292821