chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148109205481092055AAT32GENIChomozygous48809042
148109223381092234GA20GENIChomozygous48809044
148109320281093206TTTT----25GENIChomozygous48809046
148109373881093739A-24GENICpossibly homozygous48809050
148109497481094975CT32GENIChomozygous48809054
148109524781095248T-22GENIChomozygous48809056
148109598381095984GA32GENIChomozygous48809058
148109606081096061GA32GENIChomozygous48809062
148109623281096233TC24GENIChomozygous48809064
148109654281096543CT15GENIChomozygous48809065
148109740781097408CT35GENIChomozygous48809067
148109809681098097AT29GENIChomozygous48809069
148109827381098274TTTTC24GENICheterozygous49016118
148109827381098274TTC24GENICpossibly homozygous48809071
148109829081098291CT32GENIChomozygous48809072
148109925081099251CT9GENIChomozygous48809074
148109450581094507CT--30GENICheterozygous49316047
148109330381093313GAGAGAGAGG----------10GENICheterozygous49468576
148109446981094470GGGAGAGAGAGAGAGAGA8GENICheterozygous49316045
148109450181094502AAGAGAGAGAGAGAGAGAG26GENICheterozygous49316046