chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150852223150852224AG7GENIChomozygous56899437
5150852482150852483TC5GENIChomozygous55794700
5150853342150853343GA8GENICheterozygous56899439
5150854649150854650CG22GENIChomozygous56899441
5150854826150854827CT5GENICheterozygous56899443
5150854917150854918TTC10GENIChomozygous55794702
5150855468150855469CT19GENICpossibly homozygous56899445
5150855644150855645CT9GENICpossibly homozygous56899447
5150856822150856823TC18GENICpossibly homozygous55794704
5150861254150861255TC9GENICheterozygous55794705
5150861994150861995GA9GENIChomozygous56899449
5150862573150862574TG21GENICpossibly homozygous55794707
5150862814150862815AG7GENIChomozygous55794708
5150863651150863652TC26GENIChomozygous55794709
5150863978150863979CG19GENIChomozygous56899451
5150864024150864025GA14GENICpossibly homozygous56899453
5150864055150864056TC12GENIChomozygous55794710
5150864140150864141GA14GENIChomozygous56899455
5150868793150868794TC12GENIChomozygous55794711
5150869266150869267G-13GENIChomozygous56899457
5150869676150869677CT16GENICpossibly homozygous56899459
5150871332150871333A-8GENIChomozygous55794718
5150871508150871509CT12GENICheterozygous56899461
5150871739150871740TC10GENIChomozygous56128880
5150871940150871941CT16GENIChomozygous56899463
5150872758150872759TTTTG8GENICpossibly homozygous56899467
5150873017150873018CG1GENIChomozygous55794722
5150873333150873334AG2GENIChomozygous56128884
5150873346150873347AG1GENIChomozygous56128886
5150873491150873492GA8GENIChomozygous55794724
5150873785150873786GA1GENIChomozygous56128891
5150875288150875289TC14GENIChomozygous55794727
5150876180150876181CT6GENIChomozygous56899469
5150876339150876340AACCCAGG1GENIChomozygous55794729
5150876583150876589CCCCCC------2GENIChomozygous56899471
5150876591150876592CCAT4GENICheterozygous56899473
5150876830150876831AG10GENICpossibly homozygous55794732
5150876900150876901AC13GENICpossibly homozygous56899475
5150876941150876942CCCTTT1GENIChomozygous55794733