chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141386549141386550AC45GENIChomozygous118361602
7141387051141387052TC31GENIChomozygous118420748
7141387102141387103CT37GENIChomozygous118361603
7141387611141387612AG54GENIChomozygous118361604
7141391660141391661CT37GENIChomozygous118361605
7141392563141392564TG51GENIChomozygous118361606
7141393874141393875TC41GENIChomozygous118361607
7141397950141397951GA64GENIChomozygous118361608
7141399798141399799GA49GENIChomozygous118361609
7141400239141400240CT46GENIChomozygous118361610
7141405680141405681CT42GENIChomozygous118361611
7141407114141407115GA47GENIChomozygous118361612
7141407815141407816AG33GENIChomozygous118361613
7141410280141410281TG37GENIChomozygous118361614
7141410541141410542GC39GENIChomozygous118361615
7141411375141411376TC42GENIChomozygous118361616
7141411923141411924AG45GENIChomozygous118420749
7141401573141401574T35GENIChomozygous129940017
7141405284141405286AC8GENICpossibly homozygous133174085
7141410416141410417A28GENICheterozygous128529506
7141409088141409089AT34GENIChomozygous118434110
7141409356141409362TTGTTC34GENIChomozygous131435150
7141411840141411840TACA42GENIChomozygous131435151
7141412148141412163AACCAAACCAACCAA36GENIChomozygous131435152
7141412617141412617CTATGTAT39GENIChomozygous131435153
7141412794141412795GA40GENIChomozygous118434112
7141414632141414633GA50GENIChomozygous118361617
7141415322141415323CT31GENIChomozygous118361618
7141419199141419200TC32GENIChomozygous118361619
7141420858141420858TA36GENIChomozygous131435154
7141410091141410092TC46GENIChomozygous115939955
7141412395141412396AG25GENIChomozygous115939958
7141412476141412477TC43GENIChomozygous115939959
7141412379141412380TC24GENIChomozygous118533839
7141412420141412421AG27GENIChomozygous131441033
7141418470141418471T35GENICheterozygous130765643