chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65171576951715770GA9GENIChomozygous114799431
65171624951716250GA28GENIChomozygous114799432
65171822051718221TC25GENIChomozygous114799433
65171913751719138CT30GENIChomozygous114799434
65172187351721874AG38GENIChomozygous114799436
65172205951722060TC34GENIChomozygous114799437
65172262351722624AG25GENIChomozygous114799438
65172546351725464CT17GENIChomozygous114799439
65172573551725736CA30GENIChomozygous114799440
65172574551725746AG29GENICpossibly homozygous114799441
65172847451728475TC21GENIChomozygous114799442
65172859351728594AT39GENIChomozygous114799443
65172869651728697CT32GENIChomozygous114799444
65173011451730115AG17GENIChomozygous114799445
65173073251730733CT6GENIChomozygous114799446
65173828451738285TC19GENIChomozygous114799447