chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5154920469154920470GGCT6GENIChomozygous55803774
5154920475154920476AC8GENIChomozygous55803775
5154920483154920484CA10GENICpossibly homozygous55803776
5154920487154920488GC9GENIChomozygous55803777
5154920492154920493GC7GENIChomozygous55803778
5154920503154920504GC7GENIChomozygous55803779
5154920507154920508GC7GENIChomozygous55803780
5154920519154920520GGA6GENIChomozygous55803781
5154920531154920532CA12GENIChomozygous55803782
5154920537154920538CA12GENIChomozygous55803783
5154920543154920544GC12GENIChomozygous55803784
5154920548154920549GT14GENIChomozygous55803785
5154920574154920575GC17GENIChomozygous55803786
5154920604154920605GT26GENIChomozygous55803787
5154920647154920648AG36GENIChomozygous55803788
5154920650154920651AG38GENIChomozygous55803789
5154943909154943910A-25GENICheterozygous55803790
5154949402154949403CCT3INTERGENICheterozygous55803791
5154950372154950373A-23INTERGENICheterozygous55803792
5154954034154954035A-20INTERGENICheterozygous55803793
5154958935154958936GGA43INTERGENIChomozygous55803794
5154958967154958968T-29INTERGENIChomozygous55803795
5154961556154961557T-20INTERGENICheterozygous55803796
5154961634154961638AAGG----12INTERGENIChomozygous55803797
5154962106154962107CCT28INTERGENIChomozygous55803798