chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83751612737516128AC4GENICheterozygous52584893
83751615937516160AC5GENICheterozygous52584894
83752179037521791TC11GENIChomozygous52584895
83752186837521869CCTTT5GENIChomozygous52584896
83760371337603714AG9GENICheterozygous52584897
83760374737603748GT7GENICheterozygous52584898
83760375737603758TA7GENICheterozygous52584899
83760391237603913GT21GENICpossibly homozygous52584900
83760394337603944CT14GENICheterozygous52584901
83765104337651044GGA9GENICheterozygous52584902
83765106537651066CCA12GENICheterozygous52584903
83765107937651080AG19GENICheterozygous52584904
83765110437651105GA23GENICheterozygous52584905
83765111237651113AT22GENICheterozygous52584906
83765111537651116CT22GENICheterozygous52584907
83765114037651141GA32GENICheterozygous52584908
83765115937651160AG33GENICheterozygous52584909
83765126337651264CT28GENICheterozygous52584910
83765126837651269TA27GENICheterozygous52584911
83765128937651290CT26GENICheterozygous52584912
83765129137651292GA26GENICheterozygous52584913
83765145137651452CA33GENICheterozygous52584914
83765147637651477AG35GENICheterozygous52584915
83765151737651518CA34GENICheterozygous52584916
83765154237651543TA4GENIChomozygous52584917
83765154237651543TC20GENIChomozygous52584918
83765157137651572GGT12GENICheterozygous52584919
83765157137651572GGA12GENICheterozygous52584920
83765158837651589TA15GENICheterozygous52584921
83765159037651591CCT7GENIChomozygous52584922
83765159337651595TG--6GENIChomozygous52584923
83765161237651613GC8GENICheterozygous52584924
83765161937651620GC6GENICheterozygous52584925
83765163537651636CA6GENIChomozygous52584926
83765165337651654CA1GENIChomozygous52584927
83765210337652104CA89GENICheterozygous52584928
83765214637652147GA69GENICheterozygous52584929
83765215037652151AG65GENICheterozygous52584930
83765216537652166GT63GENICheterozygous52584931
83765262537652626GA33GENIChomozygous52584932