chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105692772456927725TC18GENIChomozygous116784627
105692782256927823CT18GENIChomozygous116784629
105692783556927836TC19GENIChomozygous116784631
105692797656927977CT21GENIChomozygous116784633
105692818856928189GA21GENIChomozygous116784635
105692820456928205GA18GENIChomozygous116784637
105692826956928270TC25GENIChomozygous116784639
105692828656928287TC26GENIChomozygous116784641
105692831056928311TC27GENIChomozygous116784643
105692845456928455CT32GENIChomozygous116784645
105692866356928664AG44GENIChomozygous116784647
105692867856928679CA44GENIChomozygous116784649
105692873556928736GA35GENIChomozygous116784651
105692877156928772GA35GENIChomozygous116784653
105692882156928822CT36GENIChomozygous116784655
105692893756928938TC36GENIChomozygous116784657
105692918756929188GA21GENIChomozygous116784659
105692920156929202AG19GENIChomozygous116784661
105692930856929309AG19GENIChomozygous116784663
105692935756929358TC12GENIChomozygous116784665
105692939656929397AG16GENIChomozygous116784667
105692977856929779TG19GENIChomozygous116784669
105692977956929780CA19GENIChomozygous116784671
105692993556929936TC24GENIChomozygous116784673
105692995856929959GT29GENIChomozygous116784677
105692997756929978TC28GENIChomozygous116784679
105693010056930101GA21GENIChomozygous116784681
105693016156930162CT22GENIChomozygous116784683
105693019956930200TA30GENIChomozygous117060006
105693021656930217AT22GENIChomozygous117060008
105693048356930484GA35GENIChomozygous116784685
105693089656930897GA28GENIChomozygous116784689
105693093356930934CT22GENIChomozygous116784693
105693133356931334GA23GENIChomozygous116603032
105693267556932676CT21GENIChomozygous117060010