chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105692772456927725TC21GENIChomozygous116784627
105692782256927823CT21GENIChomozygous116784629
105692783556927836TC20GENIChomozygous116784631
105692797656927977CT20GENIChomozygous116784633
105692818856928189GA14GENIChomozygous116784635
105692820456928205GA11GENIChomozygous116784637
105692826956928270TC16GENIChomozygous116784639
105692828656928287TC16GENIChomozygous116784641
105692831056928311TC22GENIChomozygous116784643
105692845456928455CT16GENIChomozygous116784645
105692866356928664AG23GENIChomozygous116784647
105692867856928679CA24GENIChomozygous116784649
105692873556928736GA20GENIChomozygous116784651
105692877156928772GA25GENIChomozygous116784653
105692882156928822CT25GENIChomozygous116784655
105692893756928938TC21GENIChomozygous116784657
105692918756929188GA24GENIChomozygous116784659
105692920156929202AG24GENIChomozygous116784661
105692930856929309AG26GENIChomozygous116784663
105692935756929358TC24GENIChomozygous116784665
105692939656929397AG21GENIChomozygous116784667
105692941356929414AG18GENIChomozygous116935930
105692977856929779TG23GENIChomozygous116784669
105692977956929780CA23GENIChomozygous116784671
105692993556929936TC20GENIChomozygous116784673
105692995856929959GT23GENIChomozygous116784677
105692997756929978TC23GENIChomozygous116784679
105693010056930101GA23GENIChomozygous116784681
105693016156930162CT18GENIChomozygous116784683
105693048356930484GA15GENICpossibly homozygous116784685
105693084756930848CT23GENIChomozygous116784687
105693089656930897GA19GENIChomozygous116784689
105693093356930934CT21GENIChomozygous116784693
105693104256931043CG24GENIChomozygous116935932
105693360356933604GA15GENIChomozygous116935934
105693455956934560GA15GENIChomozygous116935936
105693508656935087GA19GENIChomozygous116603059