chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135062002950620030CT50INTERGENIChomozygous114340886
135062023650620237TC40INTERGENIChomozygous114340888
135062224550622246CT60INTERGENIChomozygous114340890
135062536550625366TC70INTERGENIChomozygous114340892
135062542250625423GA61INTERGENIChomozygous114340894
135062744150627442CT47INTERGENIChomozygous114340896
135062798850627989GA26INTERGENIChomozygous114340898
135062857050628571TC49INTERGENIChomozygous114340900
135062857350628574CT48INTERGENIChomozygous114340902
135062919050629191CT42INTERGENICpossibly homozygous114340904
135062930250629303CT35INTERGENIChomozygous114340906
135063039550630396AG46INTERGENIChomozygous114340908
135063079850630799CT27INTERGENIChomozygous114549966
135063099550630996CT51INTERGENIChomozygous114340910
135063141250631413TC61INTERGENIChomozygous114340912
135063219950632200AT43INTERGENIChomozygous114340914
135063220450632205GC43INTERGENIChomozygous114340916
135063228950632290TA49INTERGENIChomozygous114340918
135063240850632409AC37INTERGENIChomozygous114340920
135063245650632457TC32INTERGENIChomozygous114340922
135063373150633732CT42INTERGENIChomozygous114340924
135063507650635077CT32INTERGENIChomozygous114340926
135063588750635888TG56INTERGENICpossibly homozygous114340928