chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105692772456927725TC17GENIChomozygous116784627
105692782256927823CT14GENIChomozygous116784629
105692783556927836TC14GENIChomozygous116784631
105692797656927977CT35GENIChomozygous116784633
105692818856928189GA31GENIChomozygous116784635
105692820456928205GA29GENIChomozygous116784637
105692826956928270TC26GENIChomozygous116784639
105692828656928287TC26GENIChomozygous116784641
105692831056928311TC27GENIChomozygous116784643
105692866356928664AG26GENIChomozygous116784647
105692867856928679CA25GENIChomozygous116784649
105692873556928736GA18GENIChomozygous116784651
105692877156928772GA26GENIChomozygous116784653
105692882156928822CT29GENIChomozygous116784655
105692893756928938TC22GENIChomozygous116784657
105692918756929188GA33GENIChomozygous116784659
105692920156929202AG32GENIChomozygous116784661
105692930856929309AG23GENIChomozygous116784663
105692935756929358TC20GENIChomozygous116784665
105692939656929397AG16GENIChomozygous116784667
105692941356929414AG9GENIChomozygous116935930
105692977856929779TG27GENIChomozygous116784669
105692977956929780CA26GENIChomozygous116784671
105692993556929936TC35GENIChomozygous116784673
105692995856929959GT35GENIChomozygous116784677
105692997756929978TC38GENIChomozygous116784679
105693010056930101GA25GENIChomozygous116784681
105693016156930162CT27GENIChomozygous116784683
105693048356930484GA11GENIChomozygous116784685
105693084756930848CT20GENIChomozygous116784687
105693089656930897GA33GENIChomozygous116784689
105693093356930934CT34GENIChomozygous116784693
105693104256931043CG31GENIChomozygous116935932
105693360356933604GA24GENIChomozygous116935934
105693455956934560GA26GENIChomozygous116935936
105693508656935087GA16GENIChomozygous116603059