chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138380537983805380TC29GENIChomozygous956097935
138380582683805827AT45GENIChomozygous956097936
138380593283805933TC36GENIChomozygous956097937
138380617183806172GT18GENIChomozygous956097938
138380617783806178CG17GENIChomozygous956097939
138380618083806181TA18GENIChomozygous956097940
138380631183806312GA20GENIChomozygous956097941
138380649383806494AG35GENIChomozygous956097942
138380797083807971GA35GENIChomozygous956097943
138380825083808251GC46GENIChomozygous956097944
138380998783809988CT28GENIChomozygous956097945
138381109483811095GA39GENIChomozygous956097946
138381126883811269TC36GENIChomozygous956097947
138381239083812391GA14GENIChomozygous956097948
138381425383814254AG39GENIChomozygous956097949
138381451583814516GA22GENIChomozygous956097950
138381473483814735TC20GENIChomozygous956097951
138381557483815575CA37GENIChomozygous956097952
138381582383815824AG27GENIChomozygous956097953
138381692183816922TC30GENIChomozygous956097954
138382143883821439AT25GENIChomozygous956097955
138382156883821569GC25GENIChomozygous956097956
138382161383821614GT28GENIChomozygous956097957
138382177683821777GC21GENIChomozygous956097958
138382266383822664GA46GENIChomozygous956097959
138382777383827774GA40GENIChomozygous956097960
138382841683828417TG10GENIChomozygous956097961
138382857883828579TG18GENIChomozygous956097962
138382872283828723GA22GENIChomozygous956097963
138383136683831367TC18GENIChomozygous956097964
138383433183834332AG35GENIChomozygous956097965
138383479383834794TC45GENIChomozygous956097966
138383514083835141AG18GENIChomozygous956097967
138383615483836155AG21GENICpossibly homozygous956097968
138383662283836623AT22GENICpossibly homozygous956097969
138383686283836863TA28GENIChomozygous956097970