chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X111887887111887888AT2GENIChomozygous45550635
X111887891111887892TTGGTAGAGCG3GENIChomozygous45550637
X111887893111887894TTTG3GENIChomozygous45573151
X111887897111887898AAGCAAG3GENIChomozygous45573153
X111887900111887901G-3GENIChomozygous45573155
X111891965111891966CCA10GENICheterozygous45195286
X111893839111893840G-4GENIChomozygous45195291
X111895577111895578TTA14GENICheterozygous45195296
X111899846111899847T-19GENIChomozygous45195304
X111899923111899927CACA----10GENICheterozygous45594972
X111899925111899927CA--10GENICheterozygous45520860
X111901060111901061TG5GENIChomozygous45195309
X111901908111901909GT17GENIChomozygous45195311
X111902561111902565CACA----3GENICheterozygous45520862
X111902563111902565CA--3GENICheterozygous45520864
X111904539111904541AC--20GENICheterozygous45520866
X111910906111910907TTAA3GENICheterozygous45195322
X111918855111918856A-16GENICheterozygous45520868
X111944105111944106T-10INTERGENICheterozygous45550639