chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148109205481092055AAT27GENIChomozygous48809042
148109223381092234GA12GENIChomozygous48809044
148109320281093206TTTT----18GENIChomozygous48809046
148109330381093313GAGAGAGAGG----------4GENICheterozygous49468576
148109373881093739A-20GENICpossibly homozygous48809050
148109446981094470GGGAGAGAGAGAGAGAGA4GENICheterozygous49316045
148109497481094975CT21GENIChomozygous48809054
148109524781095248T-14GENIChomozygous48809056
148109598381095984GA14GENIChomozygous48809058
148109606081096061GA25GENIChomozygous48809062
148109623281096233TC29GENIChomozygous48809064
148109654281096543CT19GENICpossibly homozygous48809065
148109740781097408CT18GENIChomozygous48809067
148109752481097525CCT23GENICheterozygous49016116
148109809681098097AT28GENIChomozygous48809069
148109827381098274TTTTC20GENICheterozygous49016118
148109827381098274TTC20GENICpossibly homozygous48809071
148109829081098291CT21GENIChomozygous48809072
148109925081099251CT5GENIChomozygous48809074