chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105692772456927725TC54GENIChomozygous116784627
105692782256927823CT49GENIChomozygous116784629
105692783556927836TC47GENIChomozygous116784631
105692797656927977CT55GENIChomozygous116784633
105692818856928189GA47GENIChomozygous116784635
105692820456928205GA44GENIChomozygous116784637
105692826956928270TC54GENIChomozygous116784639
105692828656928287TC50GENIChomozygous116784641
105692831056928311TC58GENIChomozygous116784643
105692845456928455CT65GENIChomozygous116784645
105692866356928664AG45GENIChomozygous116784647
105692867856928679CA46GENIChomozygous116784649
105692873556928736GA58GENICpossibly homozygous116784651
105692877156928772GA56GENIChomozygous116784653
105692882156928822CT51GENIChomozygous116784655
105692893756928938TC51GENIChomozygous116784657
105692918756929188GA59GENIChomozygous116784659
105692920156929202AG55GENIChomozygous116784661
105692930856929309AG57GENIChomozygous116784663
105692935756929358TC63GENIChomozygous116784665
105692939656929397AG57GENIChomozygous116784667
105692941356929414AG55GENIChomozygous116935930
105692977856929779TG56GENIChomozygous116784669
105692977956929780CA56GENIChomozygous116784671
105692993556929936TC49GENIChomozygous116784673
105692995856929959GT46GENIChomozygous116784677
105692997756929978TC45GENIChomozygous116784679
105693010056930101GA54GENIChomozygous116784681
105693016156930162CT54GENIChomozygous116784683
105693019956930200TA53GENIChomozygous117060006
105693021656930217AT50GENIChomozygous117060008
105693023356930233G48GENIChomozygous131094656
105693048356930484GA33GENIChomozygous116784685
105693064456930644TAC26GENIChomozygous131094657
105693089656930897GA43GENIChomozygous116784689
105693093356930934CT44GENIChomozygous116784693
105693133356931334GA40GENIChomozygous116603032
105693267556932676CT57GENIChomozygous117060010