chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1767882366788237AC42GENIChomozygous110941782
1767884446788445CT37GENIChomozygous110941784
1767887066788707AG30GENIChomozygous110941786
1767888806788881CT31GENIChomozygous110941788
1767901006790101GC39GENIChomozygous110941790
1767904516790452GA23GENIChomozygous110941792
1767910356791036GT21GENIChomozygous110941794
1767934296793430CT47GENIChomozygous110941796
1767942116794212AG47GENIChomozygous110941798
1767959926795993GA15GENIChomozygous110941801
1767963096796310CT31GENIChomozygous110941803
1767968216796822CG42GENIChomozygous110941805
1768003226800323AC29GENIChomozygous110941807
1768003526800353CT29GENIChomozygous110941809
1768004276800428CT29GENIChomozygous110941811
1768004596800460CT29GENIChomozygous110941813
1768053366805337AG28GENIChomozygous110941815
1768073606807361CA36GENIChomozygous110941817
1768073676807368CA35GENIChomozygous110941819
1768076036807604AT24GENIChomozygous110941821
1768092806809281AG37GENIChomozygous110941823
1768107286810729AC47GENIChomozygous110941825
1768109276810928AG44GENIChomozygous110941827
1768109296810930TG43GENIChomozygous110941829
1768112486811249TC27GENIChomozygous110941831
1768117176811718GC25GENIChomozygous110941833
1768148076814808AG19GENIChomozygous110941835
1768156706815671AT49GENIChomozygous110941837
1768157356815736AG49GENIChomozygous110941839
1768160406816041CT27GENIChomozygous110941841
1768167876816788TG31GENIChomozygous110941843
1768170566817057CT26GENIChomozygous110941845
1768171966817197GT18GENIChomozygous110941847
1768179956817996TG37GENIChomozygous110941849
1768187066818707AG14GENIChomozygous110941851
1768196556819656GA23GENIChomozygous110941853
1768200686820069AG29GENIChomozygous110941855
1768229046822905TC37GENIChomozygous110941857