chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105557203955572039A13GENICheterozygous131094347
105557227155572272AG21GENIChomozygous116934859
105557271855572719AG23GENIChomozygous116782666
105557290855572909T22GENIChomozygous131094348
105557307255573073AG16GENIChomozygous116934861
105557331255573313A16GENIChomozygous131094349
105557399055573991GA18GENIChomozygous116934863
105557497655574977TA29GENIChomozygous116978011
105557579755575798AG29GENIChomozygous116934865
105557579855575799CT29GENIChomozygous116602605
105557627655576277AT24GENIChomozygous116602607
105557655655576557GA23GENIChomozygous116934867
105557656155576561GA23GENIChomozygous131094350
105557758655577587GA23GENIChomozygous116934869
105557801755578018AG13GENIChomozygous116934871
105558141755581418AC11GENIChomozygous116602611
105558305555583056TC24GENIChomozygous116602613
105558348455583485AG27GENIChomozygous116602615
105558520055585201AG17GENIChomozygous116602619
105558661255586613AG17GENIChomozygous116602623
105558763555587636TC20GENIChomozygous116602625
105559043055590431CT16GENIChomozygous116602627
105559197955591986TGTTTTT28GENIChomozygous131094351
105559301355593014CT16GENIChomozygous116890218
105558002055580020AAGCAAAGCAACAT24GENIChomozygous128818963
105558518455585184GGGCGGGTAGTGAGTGT11GENIChomozygous128818965
105558949955589499GAG14GENIChomozygous128818966