chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146181600146181601TC30GENIChomozygous112872150
4146181886146181887AG19GENIChomozygous112872151
4146181978146181979CT33GENIChomozygous113179426
4146182137146182138GA14GENIChomozygous112872153
4146183724146183725CT16GENIChomozygous113179427
4146183979146183980CT34GENIChomozygous113179428
4146185579146185580GA23GENIChomozygous113179429
4146185681146185682AC28GENIChomozygous112872155
4146188627146188628GA37GENIChomozygous113179430
4146190659146190660CT27GENIChomozygous113242329
4146193170146193171GC29GENIChomozygous113179431
4146194372146194373AT21GENIChomozygous119359195
4146194601146194602TC28GENIChomozygous112872159
4146195173146195174GA24GENIChomozygous113179432
4146195782146195783TC33GENIChomozygous113179433
4146197724146197725CA34GENIChomozygous113179435
4146200743146200744GA30GENIChomozygous113179438
4146201657146201658GT31GENIChomozygous113179439
4146202487146202488CT18GENIChomozygous113179440