chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105692772456927725TC44GENIChomozygous116784627
105692782256927823CT47GENIChomozygous116784629
105692783556927836TC45GENIChomozygous116784631
105692797656927977CT41GENIChomozygous116784633
105692818856928189GA57GENIChomozygous116784635
105692820456928205GA56GENIChomozygous116784637
105692826956928270TC59GENIChomozygous116784639
105692828656928287TC59GENIChomozygous116784641
105692831056928311TC50GENIChomozygous116784643
105692837956928380TG46GENICheterozygous118123660
105692845456928455CT58GENICpossibly homozygous116784645
105692866356928664AG49GENIChomozygous116784647
105692867856928679CA44GENIChomozygous116784649
105692873556928736GA52GENIChomozygous116784651
105692877156928772GA63GENIChomozygous116784653
105692882156928822CT47GENICpossibly homozygous116784655
105692893756928938TC50GENIChomozygous116784657
105692918756929188GA61GENIChomozygous116784659
105692920156929202AG61GENIChomozygous116784661
105692930856929309AG51GENIChomozygous116784663
105692935756929358TC43GENIChomozygous116784665
105692939656929397AG33GENIChomozygous116784667
105692941356929414AG27GENIChomozygous116935930
105692977856929779TG44GENIChomozygous116784669
105692977956929780CA43GENICpossibly homozygous116784671
105692993556929936TC35GENIChomozygous116784673
105692995856929959GT30GENIChomozygous116784677
105692997756929978TC34GENIChomozygous116784679
105693010056930101GA43GENICpossibly homozygous116784681
105693016156930162CT47GENIChomozygous116784683
105693048356930484GA51GENIChomozygous116784685
105693084756930848CT39GENIChomozygous116784687
105693089656930897GA47GENIChomozygous116784689
105693093356930934CT58GENIChomozygous116784693
105693104256931043CG42GENIChomozygous116935932
105693360356933604GA46GENIChomozygous116935934
105693455956934560GA49GENIChomozygous116935936
105693508656935087GA43GENICpossibly homozygous116603059