chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157144997157144998TC17GENIChomozygous112905592
4157145282157145283GA23GENIChomozygous112905596
4157145362157145363TC22GENIChomozygous112905598
4157145639157145640AG37GENICpossibly homozygous112905599
4157145756157145757GA29GENIChomozygous112905601
4157145862157145863GA22GENIChomozygous112905603
4157146025157146026AT22GENIChomozygous112905605
4157146155157146156GA31GENIChomozygous112905607
4157146176157146177TC20GENIChomozygous112905609
4157146181157146182AT19GENIChomozygous112905611
4157146242157146243CA27GENIChomozygous119317539
4157149886157149887GC41GENICheterozygous112905625
4157150960157150961GA45GENICheterozygous112905632
4157150963157150964AC47GENICheterozygous112905634
4157151133157151134AG34GENICheterozygous112905640
4157154870157154871CA24GENIChomozygous119317540