chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121564592415645925GA20GENIChomozygous139092227
121564663715646638GA57GENIChomozygous139092228
121564688815646889TC37GENIChomozygous139092229
121564868115648682CT48GENIChomozygous142320683
121565071815650719CA51GENIChomozygous142320684
121565227215652273AC50GENIChomozygous139092230
121565252715652528TC35GENIChomozygous139092232
121565530815655309AG49GENIChomozygous139092233
121565559315655594CT56GENICpossibly homozygous139092234
121565639615656397AC33GENICpossibly homozygous142320685
121565679915656800GA56GENIChomozygous139092235
121565796015657961GA38GENIChomozygous142320686
121565839115658392CT45GENIChomozygous142320687
121565850515658506CA44GENIChomozygous142320688
121565866615658667CT53GENIChomozygous142320689
121566008715660088GC48GENIChomozygous142320690
121566048815660489AG50GENIChomozygous142320691
121566207215662073CA46GENICpossibly homozygous142320692
121566248015662481AG51GENIChomozygous142320693
121566284115662842CT43GENIChomozygous142320694
121566295315662954CT58GENIChomozygous142320695
121566306215663063CT59GENIChomozygous142320696
121566330515663306AG26GENIChomozygous139092238
121566356615663567AG52GENIChomozygous139092239
121566367715663678GC37GENIChomozygous139092240
121566405515664056CT57GENIChomozygous142320697
121566445415664455CT50GENIChomozygous142320698
121566450315664504AG50GENIChomozygous139092241
121566458515664586GC51GENIChomozygous142320699
121566462915664630GA42GENIChomozygous142320700
121566520315665204CT50GENIChomozygous142320701
121566542315665424CT57GENIChomozygous142320702
121566694715666948CT29GENIChomozygous139092243
121566369715663697ACCATCCTATGTCCAGTTCACCCTTTCTTTGCTGACGCTCTTC21GENIChomozygous142309585
121566699715666997T37GENIChomozygous142309586