chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121564592415645925GA10GENIChomozygous139092227
121564663715646638GA7GENIChomozygous139092228
121564688815646889TC6GENIChomozygous139092229
121565227215652273AC17GENIChomozygous139092230
121565252715652528TC9GENIChomozygous139092232
121565530815655309AG19GENIChomozygous139092233
121565559315655594CT12GENIChomozygous139092234
121565679915656800GA20GENIChomozygous139092235
121565796015657961GA10GENIChomozygous142320686
121564868115648682CT8GENIChomozygous142320683
121565071815650719CA11GENIChomozygous142320684
121565639615656397AC13GENIChomozygous142320685
121565839115658392CT17GENIChomozygous142320687
121565850515658506CA18GENIChomozygous142320688
121565866615658667CT21GENIChomozygous142320689
121566008715660088GC20GENIChomozygous142320690
121566048815660489AG26GENIChomozygous142320691
121566207215662073CA14GENIChomozygous142320692
121566248015662481AG14GENIChomozygous142320693
121566284115662842CT22GENIChomozygous142320694
121566295315662954CT19GENIChomozygous142320695
121566306215663063CT20GENIChomozygous142320696
121566330515663306AG8GENIChomozygous139092238
121566356615663567AG17GENIChomozygous139092239
121566367715663678GC12GENIChomozygous139092240
121566405515664056CT18GENIChomozygous142320697
121566445415664455CT26GENIChomozygous142320698
121566450315664504AG22GENIChomozygous139092241
121566458515664586GC18GENIChomozygous142320699
121566462915664630GA21GENIChomozygous142320700
121566520315665204CT14GENIChomozygous142320701
121566542315665424CT13GENIChomozygous142320702
121566694715666948CT7GENIChomozygous139092243
121566699715666997T12GENICpossibly homozygous142309586
121565948915659495TGTGTA13GENICheterozygous142309584
121566369715663697ACCATCCTATGTCCAGTTCACCCTTTCTTTGCTGACGCTCTTC7GENIChomozygous142309585