chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57637674976376750GC35INTERGENIChomozygous812053511
57637702176377022AG14INTERGENIChomozygous812053512
57639216776392168GA29GENIChomozygous812053513
57639267476392675GA12GENIChomozygous812053514
57639287276392873GA14GENIChomozygous812053515
57639496676394967CT13GENIChomozygous812053516
57639738276397383CG33GENIChomozygous812053517
57639753176397532GA18GENIChomozygous812053518
57640109976401100CT31GENIChomozygous812053519
57640495376404954CT18GENIChomozygous812053520
57640539176405392CT24GENIChomozygous812053521
57641207876412079AG24GENIChomozygous812053522
57641221276412213CT22GENIChomozygous812053523
57641570576415706CT24GENIChomozygous812053524
57641587376415874AG55GENIChomozygous812053525
57641598576415986GT50GENIChomozygous812053526
57641607876416079CT11GENIChomozygous812053527
57641630176416302CT63GENIChomozygous812053528
57641632276416323CG78GENIChomozygous812053529
57641643076416431TA118GENICheterozygous812053530
57641647676416477GA119GENICheterozygous812053531
57641652476416525AG99GENICheterozygous812053532
57641752276417523GT24GENIChomozygous812053533
57641881076418811CT24GENICheterozygous812053534