chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154631794346317944TC13GENIChomozygous113225622
154631824246318243GA12GENIChomozygous112679550
154631841046318411GT21GENIChomozygous112679552
154631843946318440AC29GENIChomozygous112679554
154631848146318482GA26GENIChomozygous112679556
154631850846318509TC8GENICheterozygous125855806
154631850946318510GA9GENIChomozygous125855807
154631866246318663CT13GENIChomozygous112679558
154631870846318709AT21GENIChomozygous112679560
154631876846318769AC21GENIChomozygous112679562
154631898646318987TC5GENICheterozygous125855808
154631901946319020TC9GENIChomozygous112679564
154631904246319043GC14GENIChomozygous112679566
154631924546319246TG14GENIChomozygous112679568
154631937946319380CG21GENIChomozygous112679570
154631957646319577TC8GENIChomozygous112679572
154631978046319781AG5GENIChomozygous113169594
154631978246319783CA4GENIChomozygous112679574
154631992046319921CT19GENIChomozygous112679576
154632022846320229AG12GENIChomozygous113169596
154632067246320673GT20GENIChomozygous113169598
154632107346321074GA17GENIChomozygous112679586
154632130346321304GA20GENIChomozygous112679588
154632202646322027CG11GENIChomozygous112679592
154632742246327423AG18GENIChomozygous113261589
154633033646330337GA16GENIChomozygous113225623
154633158146331582AG13GENIChomozygous112679612
154633263246332633GA17GENIChomozygous113225624
154633540846335409GA20GENIChomozygous113225625
154633558446335585CT12GENIChomozygous113261591
154633601346336014TA13GENIChomozygous113225626
154633705946337060GC14GENIChomozygous113225627