chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84389321643893217CA16GENIChomozygous52609681
84389337943893380GT9GENIChomozygous52609683
84389364343893644CA11GENIChomozygous53104801
84389374743893750TCT---2GENIChomozygous52609685
84389430843894309CA6GENIChomozygous53428612
84389430943894310AC6GENIChomozygous53428614
84389433143894332CT8GENIChomozygous53269869
84389460743894608AG5GENIChomozygous52609687
84389463443894635T-9GENIChomozygous52609689
84389473843894739AG1GENIChomozygous52609691
84389474343894744TG1GENIChomozygous52609693
84389474443894745TC1GENIChomozygous52609695
84389501443895015CT10GENICpossibly homozygous53104802
84389513043895131AAC6GENIChomozygous53104803
84389589743895898TC9GENICpossibly homozygous53104804
84389607643896077A-5GENIChomozygous52609701
84389615543896156TC12GENIChomozygous52609703
84389624743896248GA13GENICpossibly homozygous52609705