chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135308857753088578AG41GENIChomozygous114346781
135308863253088633TC48GENICpossibly homozygous114346783
135308868353088684TC48GENIChomozygous114346785
135308981953089820TC53GENIChomozygous114346787
135309019053090191TC44GENIChomozygous114346789
135309077553090776AG22GENIChomozygous114346791
135309126453091265CG27GENIChomozygous114346793
135309159653091597CG25GENIChomozygous114346795
135309159753091598GT26GENIChomozygous114346797
135309163353091634GC29GENIChomozygous114346799
135309256053092561AC35GENIChomozygous114346801
135309288953092890CT57GENIChomozygous114346803
135309301253093013AG61GENIChomozygous114346805
135309340053093401CG44GENIChomozygous114346807
135309351153093512CT47GENIChomozygous114346809
135309358153093582CT48GENIChomozygous114346811
135309386753093868AG46GENIChomozygous114346813
135309389553093896CA41GENICpossibly homozygous114346815
135309396053093961TG40GENIChomozygous114346817
135309402453094025GA45GENIChomozygous114346819
135309411453094115GA35GENIChomozygous114346821
135309413553094136AG33GENIChomozygous114346823
135309445153094452AG48GENIChomozygous114346825
135309593453095935TC44GENIChomozygous114346827
135309731853097319TC37GENIChomozygous114346829
135309760753097608CT29GENIChomozygous114346831
135309821453098215CT36GENIChomozygous114346833
135309832353098324TG37GENIChomozygous114346835
135309905253099053GC35GENIChomozygous114346837
135310170753101708GA38GENIChomozygous114346843
135309997253099973AG34GENIChomozygous114346839
135310128953101290GA43GENIChomozygous114346841
135310328653103287TC44GENIChomozygous114346845
135310455253104553TC40GENIChomozygous114346847
135310477753104778GA37GENIChomozygous114346849
135310480953104810CA36GENIChomozygous114346851
135310534053105341AG37GENIChomozygous114346853
135310756553107566AG63GENIChomozygous114346855
135310825753108258AG31GENIChomozygous114346857
135310865153108652CT35GENIChomozygous114346859