chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4175237426175237427TC12GENIChomozygous137271618
4175237920175237924AAAT17GENIChomozygous136930826
4175239092175239093AT25GENIChomozygous137271619
4175239699175239707TCTATCTA19GENIChomozygous136930827
4175239805175239806GT18GENIChomozygous137271620
4175239839175239840AG22GENIChomozygous137271621
4175240279175240280AG20GENIChomozygous137271622
4175240369175240370TC22GENIChomozygous137271623
4175240669175240670AT9GENIChomozygous137271624
4175240987175240987C15GENIChomozygous136930828
4175241112175241113AC19GENIChomozygous137271625
4175241215175241216GA18GENIChomozygous137271626
4175241246175241247TA16GENIChomozygous137271627
4175242622175242623G22GENIChomozygous136930829
4175244362175244363AG20GENIChomozygous137271628