chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17894462678944627CT27GENIChomozygous108873322
17894464678944647CT43GENIChomozygous108873323
17894471378944714GA37GENIChomozygous108873324
17894478678944787GA30GENIChomozygous108873325
17894576978945770TC38GENIChomozygous108873326
17894599078945991AG27GENIChomozygous108873327
17894874078948741CT26GENIChomozygous108873328
17894889178948892GC30GENIChomozygous108873329
17895080178950802AT28GENIChomozygous108873330
17895133378951334AG29GENIChomozygous108873331
17895294678952947CT30GENIChomozygous108873332
17895413878954139GA33GENIChomozygous108873333
17895577378955774GA31GENIChomozygous108873334
17895620978956210GA25GENIChomozygous108873335
17895682278956823CA30GENIChomozygous108873336
17896065478960655CT28GENIChomozygous108873337
17896199978962000TC32GENIChomozygous108873338
17896320178963202CT29GENIChomozygous108873339
17896364278963643GA35GENIChomozygous108873340
17896422078964221GT31GENIChomozygous108873341
17896524878965249CA17GENIChomozygous108873342
17896531278965313AG29GENIChomozygous108873343
17896705478967055TC30GENIChomozygous108873344
17896711578967116TC27GENIChomozygous108873345