chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105557203955572039A12GENIChomozygous131094347
105557227155572272AG15GENIChomozygous116934859
105557271855572719AG20GENIChomozygous116782666
105557290855572909T12GENIChomozygous131094348
105557307255573073AG13GENIChomozygous116934861
105557331255573313A12GENIChomozygous131094349
105557399055573991GA15GENIChomozygous116934863
105557497655574977TA19GENIChomozygous116978011
105557579755575798AG22GENIChomozygous116934865
105557579855575799CT22GENIChomozygous116602605
105557627655576277AT18GENIChomozygous116602607
105557655655576557GA21GENIChomozygous116934867
105557656155576561GA21GENIChomozygous131094350
105557758655577587GA15GENIChomozygous116934869
105557801755578018AG10GENIChomozygous116934871
105558002055580020AAGCAAAGCAACAT22GENIChomozygous128818963
105558141755581418AC17GENIChomozygous116602611
105558305555583056TC12GENIChomozygous116602613
105558348455583485AG21GENIChomozygous116602615
105558486155585033TAAGCTGCTGTCTCTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTTTTTACTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCTTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC12GENIChomozygous128818964
105558518455585184GGGCGGGTAGTGAGTGT2GENIChomozygous128818965
105558520055585201AG5GENIChomozygous116602619
105558661255586613AG13GENIChomozygous116602623
105558763555587636TC27GENIChomozygous116602625
105558949955589499GAG11GENIChomozygous128818966
105559043055590431CT19GENIChomozygous116602627
105559197955591986TGTTTTT23GENIChomozygous131094351
105559301355593014CT10GENIChomozygous116890218