chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138380537983805380TC33GENIChomozygous976912730
138380582683805827AT25GENIChomozygous976912731
138380593283805933TC25GENIChomozygous976912732
138380617183806172GT30GENIChomozygous976912733
138380617783806178CG29GENIChomozygous976912734
138380618083806181TA31GENIChomozygous976912735
138380631183806312GA33GENICpossibly homozygous976912736
138380649383806494AG32GENIChomozygous976912737
138380726283807263AG21GENIChomozygous976912738
138380797083807971GA21GENIChomozygous976912739
138380825083808251GC21GENIChomozygous976912740
138380998783809988CT18GENIChomozygous976912741
138381109483811095GA27GENIChomozygous976912742
138381126883811269TC19GENIChomozygous976912743
138381239083812391GA18GENIChomozygous976912744
138381425383814254AG16GENIChomozygous976912745
138381451583814516GA29GENIChomozygous976912746
138381473483814735TC17GENIChomozygous976912747
138381557483815575CA23GENIChomozygous976912748
138381582383815824AG20GENIChomozygous976912749
138381647383816474TC21GENIChomozygous976912750
138381650783816508CT16GENIChomozygous976912751
138381692183816922TC21GENIChomozygous976912752
138382143883821439AT15GENIChomozygous976912753
138382156883821569GC16GENIChomozygous976912754
138382161383821614GT25GENIChomozygous976912755
138382177683821777GC19GENIChomozygous976912756
138382266383822664GA33GENIChomozygous976912757
138382777383827774GA25GENIChomozygous976912758
138382781583827816CT30GENIChomozygous976912759
138382841683828417TG17GENIChomozygous976912760
138382857883828579TG15GENIChomozygous976912761
138382872283828723GA14GENIChomozygous976912762
138383130583831306AG3GENIChomozygous976912763
138383136683831367TC12GENIChomozygous976912764
138383433183834332AG26GENIChomozygous976912765
138383479383834794TC31GENIChomozygous976912766
138383514083835141AG18GENIChomozygous976912767
138383615483836155AG21GENIChomozygous976912768
138383686283836863TA29GENIChomozygous976912769