chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10105568635105568636TC65GENIChomozygous51761865
10105569697105569698AC64GENIChomozygous51761867
10105570222105570234GAAGTCGGGAGG------------30GENIChomozygous51761869
10105570450105570451GGGT53GENIChomozygous51761871
10105570845105570846TA73GENICpossibly homozygous51761873
10105570888105570889TA62GENICpossibly homozygous51761875
10105570890105570891AG58GENICpossibly homozygous51761877
10105571319105571320CA33GENICpossibly homozygous51761879
10105571450105571451TC35GENICheterozygous51761881
10105571459105571463ATCC----11GENICheterozygous51761883
10105571466105571467CT32GENICheterozygous51761885
10105571640105571641TC37GENIChomozygous51761887
10105571799105571800GA47GENIChomozygous51761889
10105571934105571935GA46GENIChomozygous51761891
10105572253105572254A-49GENIChomozygous51761893