chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161854729618547297CT21GENIChomozygous142533524
161854740518547406AG24GENICpossibly homozygous139888990
161854861218548613CT34GENIChomozygous139888991
161854921018549211AG22GENIChomozygous139888992
161855001218550013CT30GENIChomozygous142533525
161855011518550116GC30GENIChomozygous139888993
161855034618550347AG34GENIChomozygous139888994
161855053018550531TA31GENIChomozygous139888995
161855114918551150AG41GENIChomozygous139888997
161855186018551861TC31GENIChomozygous139888998
161855299418552995AG26GENIChomozygous139889000
161855325818553259TC15GENIChomozygous139889001
161855333318553334AG24GENIChomozygous139889002
161855346018553461TC28GENIChomozygous139889003
161855460218554603TA39GENIChomozygous139889004
161855554418555545GA31GENIChomozygous142533526
161855579718555798TC26GENIChomozygous139889005
161855314318553144C6GENIChomozygous139824633
161855614918556150CG22GENIChomozygous139889006
161855633918556340GA33GENIChomozygous139889007
161855654918556550GA33GENIChomozygous142533527
161855659118556592TC30GENIChomozygous142533528