chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123202575132025752TC25GENIChomozygous139130530
123202587832025879GA29GENIChomozygous147003753
123202593932025940GT23GENIChomozygous143542580
123202598732025991AACT21GENIChomozygous147000015
123202625232026253GA14GENIChomozygous147003754
123202664332026644TC23GENIChomozygous143542582
123202729032027291TA22GENIChomozygous147003755
123202754932027550TC23GENIChomozygous143542583
123202785632027857AG19GENIChomozygous143542584
123202828432028285GA20GENIChomozygous143542586
123202830132028302TC18GENIChomozygous139130533
123202901832029019TC22GENIChomozygous143542587
123202912232029123TC23GENIChomozygous143542588
123202980732029808CT26GENIChomozygous147003756
123202997432029975CT21GENIChomozygous147003757
123203001032030011GA18GENIChomozygous143542591
123203007632030077CT17GENIChomozygous147003758
123203028232030283AG21GENIChomozygous143542592
123203052932030530AC16GENIChomozygous143542593
123203084132030842GA14GENIChomozygous143542594
123203162632031627GA22GENIChomozygous143542595
123203166032031661CT18GENIChomozygous143542596
123203309532033096CG23GENIChomozygous139130535
123203312132033122GA20GENIChomozygous143542603
123203315332033154CT17GENIChomozygous147003759
123203353832033539GA19GENIChomozygous143542604
123203357432033575TC13GENIChomozygous147003760
123203358332033584AG14GENIChomozygous143542605
123203366032033661TC15GENIChomozygous139130536
123202618532026185TAT20GENIChomozygous139052309
123202726132027261GT17GENIChomozygous147000016
123202871532028722TGGTCAC14GENIChomozygous143522931
123203044732030455ATGTGCAC15GENIChomozygous144099031