chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141386549141386550AC27GENIChomozygous118361602
7141387051141387052TC20GENIChomozygous118420748
7141387102141387103CT21GENIChomozygous118361603
7141387611141387612AG29GENIChomozygous118361604
7141391660141391661CT8GENIChomozygous118361605
7141392563141392564TG23GENIChomozygous118361606
7141393874141393875TC15GENIChomozygous118361607
7141397950141397951GA24GENIChomozygous118361608
7141399798141399799GA32GENICpossibly homozygous118361609
7141400239141400240CT26GENIChomozygous118361610
7141401573141401574T15GENIChomozygous129940017
7141405680141405681CT14GENIChomozygous118361611
7141407114141407115GA20GENIChomozygous118361612
7141407815141407816AG16GENIChomozygous118361613
7141409356141409362TTGTTC15GENIChomozygous131435150
7141410280141410281TG13GENIChomozygous118361614
7141410541141410542GC15GENIChomozygous118361615
7141411375141411376TC16GENIChomozygous118361616
7141411840141411840TACA10GENIChomozygous131435151
7141411923141411924AG15GENIChomozygous118420749
7141412148141412163AACCAAACCAACCAA14GENIChomozygous131435152
7141412379141412380TC11GENIChomozygous118533839
7141412617141412617CTATGTAT11GENIChomozygous131435153
7141414632141414633GA21GENIChomozygous118361617
7141415322141415323CT11GENIChomozygous118361618
7141419199141419200TC19GENIChomozygous118361619
7141420858141420858TA15GENICpossibly homozygous131435154
7141409088141409089AT16GENIChomozygous118434110
7141412794141412795GA17GENIChomozygous118434112
7141410091141410092TC14GENIChomozygous115939955
7141412395141412396AG10GENIChomozygous115939958
7141412476141412477TC13GENIChomozygous115939959
7141412420141412421AG10GENIChomozygous131441033