chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86448148364481486CTT43GENIChomozygous130364081
86448208064482081GT50GENIChomozygous117043682
86448263164482631TT59GENIChomozygous130364082
86448339264483393TC47GENIChomozygous117043683
86448345764483458AC56GENIChomozygous117043684
86448376664483767GA54GENIChomozygous117043685
86448393864483939TC16GENIChomozygous117944626
86448449964484500GA47GENIChomozygous117043686
86448455064484550AA40GENIChomozygous130364085
86448494364484943CCCCA36GENIChomozygous133190185
86448545864485458AA42GENIChomozygous130364088
86448598464485999CGGGCCCCGTCCGTC46GENIChomozygous130364089
86448721464487215TC45GENIChomozygous117043689
86448721964487220AG49GENIChomozygous117043690
86448733464487335AG54GENIChomozygous117043691
86448902964489030TC67GENIChomozygous117043692
86448909064489097GTCTAAT47GENIChomozygous130364090
86448934464489345AG60GENIChomozygous117043693
86448939064489391CT69GENIChomozygous117043694
86449052764490528AT43GENIChomozygous117043695
86449133864491339AG48GENIChomozygous117043696
86449243264492433GA40GENIChomozygous117043697
86449260064492601AG50GENIChomozygous117043698
86449379864493799CT40GENIChomozygous117043699
86449543364495434GT53GENIChomozygous117043700
86449570664495707TC48GENIChomozygous117043701
86449594764495948TC56GENIChomozygous117043702
86449597764495978CT59GENIChomozygous117043703
86449669764496698GC50GENIChomozygous117043704
86449700664497007GT49GENIChomozygous117043705
86449701764497018AG46GENIChomozygous117043706
86449725464497255TC45GENIChomozygous117043707
86450034364500344GT52GENICpossibly homozygous117043708
86450103164501032GA36GENIChomozygous117043709
86450208464502085AG58GENIChomozygous117043710
86450274964502750AC40GENICpossibly homozygous117043711
86449092864490929G43GENIChomozygous130364091
86449212864492138TCGAGCTCCT52GENIChomozygous130364092
86449678664496787T57GENIChomozygous130364093
86448944864489449A62GENIChomozygous134840273