chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85291887552918875CTGTGAAGAACCATGA22GENIChomozygous130362250
85291919852919199A10GENIChomozygous132666671
85292029852920299TA27GENIChomozygous116819096
85292166152921662TC26GENIChomozygous116819098
85291928652919287TC21GENIChomozygous116819092
85292028152920282CA29GENIChomozygous116819094
85292179552921796TC22GENIChomozygous116819100
85292192352921924GC25GENIChomozygous116819102
85292192552921925T25GENIChomozygous130362251
85292200752922008TC25GENIChomozygous117917162
85292200852922009CT26GENIChomozygous117917163
85292228852922290GT27GENIChomozygous130362252
85292255352922554T23GENIChomozygous130362253
85292259652922597CT24GENIChomozygous116819104
85292259752922598AG24GENIChomozygous116819106
85292273952922740AG18GENIChomozygous116819108
85292319152923192GA35GENIChomozygous116819110
85292320852923209GA35GENIChomozygous116819112
85292340552923406CT23GENIChomozygous116819114
85292408352924084GA19GENIChomozygous116819116
85292434052924341AC29GENIChomozygous116819118
85292493152924932AG33GENIChomozygous116819120
85292495752924958TC34GENIChomozygous116819122
85292536152925362AG19GENIChomozygous116819124
85292622352926223GTCTGTCT19GENIChomozygous132666672
85292629752926298TC10GENIChomozygous116963546
85292275552922756TA21GENIChomozygous116963543
85292626852926269GA14GENIChomozygous116963545
85292656252926562A22GENIChomozygous132666673
85292703552927036CT30GENIChomozygous116963547
85292778852927788AGGAGGGGAAAAGT29GENIChomozygous128590890
85292813052928131CA35GENIChomozygous116963548
85292848352928484GT47GENICpossibly homozygous116819144
85292883652928837TC13GENIChomozygous116819154
85293444552934446AG26GENIChomozygous116819198
85293411952934120TC20GENIChomozygous116963549
85292879652928797CT13GENICheterozygous134221440
85293465952934663TGGA26GENIChomozygous132666674
85293469652934697AG26GENIChomozygous116819202
85293598852935989GA29GENIChomozygous116963553
85293647352936474A22GENIChomozygous128590891
85293657652936577TC11GENIChomozygous132672410