chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86448148364481486CTT21GENIChomozygous130364081
86448208064482081GT29GENIChomozygous117043682
86448263164482631TT26GENIChomozygous130364082
86448339264483393TC22GENIChomozygous117043683
86448376664483767GA27GENIChomozygous117043685
86448393864483939TC11GENIChomozygous117944626
86448405064484050TTGAG23GENIChomozygous130364083
86448405264484052TT25GENIChomozygous130364084
86448449964484500GA20GENIChomozygous117043686
86448455064484550AA23GENIChomozygous130364085
86448495264484952A35GENIChomozygous130364086
86448495364484953CCCT35GENIChomozygous130364087
86448545864485458AA34GENIChomozygous130364088
86448721464487215TC25GENIChomozygous117043689
86448721964487220AG24GENIChomozygous117043690
86448733464487335AG28GENIChomozygous117043691
86448902964489030TC28GENIChomozygous117043692
86448934464489345AG33GENIChomozygous117043693
86448939064489391CT31GENIChomozygous117043694
86449052764490528AT19GENIChomozygous117043695
86449133864491339AG26GENIChomozygous117043696
86448590364485904CT22GENIChomozygous117160268
86448598464485999CGGGCCCCGTCCGTC27GENIChomozygous130364089
86448909064489097GTCTAAT28GENIChomozygous130364090
86449092864490929G32GENIChomozygous130364091
86449212864492138TCGAGCTCCT19GENIChomozygous130364092
86449243264492433GA27GENIChomozygous117043697
86449260064492601AG29GENIChomozygous117043698
86449379864493799CT29GENIChomozygous117043699
86449543364495434GT25GENIChomozygous117043700
86449570664495707TC30GENIChomozygous117043701
86449594764495948TC35GENIChomozygous117043702
86449597764495978CT38GENIChomozygous117043703
86449669764496698GC22GENIChomozygous117043704
86449678664496787T26GENIChomozygous130364093
86449700664497007GT28GENIChomozygous117043705
86449701764497018AG29GENIChomozygous117043706
86449725464497255TC26GENIChomozygous117043707
86450034364500344GT27GENIChomozygous117043708
86450103164501032GA32GENIChomozygous117043709
86450208464502085AG26GENIChomozygous117043710
86450274964502750AC28GENICpossibly homozygous117043711