chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101562169515621696GT18GENIChomozygous116860680
101562181315621814AG15GENIChomozygous116860682
101562294715622948TC14GENIChomozygous116860684
101562318515623186CT12GENIChomozygous116860689
101562377915623780TC19GENIChomozygous116860691
101562410815624109CT12GENICheterozygous116860693
101562421015624211GA6GENICheterozygous116916821
101562427015624271AC21GENIChomozygous116860696
101563048515630486TC30GENIChomozygous116860698
101563081015630811TG15GENIChomozygous116976051
101563122215631223AG19GENIChomozygous116860700
101563218715632188CT19GENIChomozygous116860702
101563326015633261TC18GENIChomozygous116737849
101563480015634801CT21GENIChomozygous116860704
101563579115635792TC8GENIChomozygous116860706
101563606115636062GA25GENIChomozygous116860708
101563811615638117TG21GENIChomozygous116860710
101563866915638670CA28GENIChomozygous116860713
101563914215639143TG8GENIChomozygous116860715
101564037115640372CA25GENIChomozygous116498121
101564212015642121AG20GENIChomozygous116860718
101564266015642661CT30GENIChomozygous116860720
101564532515645326TC23GENIChomozygous116498123
101564642115646422GA21GENIChomozygous116860722
101564704115647042CT24GENIChomozygous116860724
101564809615648097TC16GENIChomozygous116498129
101564858915648590CT8GENIChomozygous118063166
101564859315648594CT8GENICheterozygous118063168
101564859715648598CT6GENICheterozygous116498131
101564901215649013CT5GENIChomozygous118031681
101565077615650777AG17GENIChomozygous116498133
101565207015652071CG6GENIChomozygous116860726
101565594815655949TC8GENIChomozygous126427093
101565707615657077CT22GENIChomozygous116860728
101565805615658057TC30GENIChomozygous116498137
101565934315659344CT15GENICheterozygous116860730
101565988715659888TC21GENIChomozygous116860732
101566042615660427AG30GENIChomozygous116860734