chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104439144144391442CT24GENIChomozygous51439634
104439161944391620TC29GENICpossibly homozygous51439638
104439167844391679TA19GENIChomozygous51439639
104439181944391820TG19GENIChomozygous51439640
104439183744391838CA18GENIChomozygous51439641
104439191844391919GA18GENICheterozygous51439644
104439194244391943AG2GENIChomozygous51439646
104439194544391946TTC3GENIChomozygous51439647
104439199744391998TTC9GENIChomozygous51439649
104439218044392181CA19GENIChomozygous51439657
104439229744392298GA26GENIChomozygous51439658