chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135262555852625559AG8GENIChomozygous114550618
135262685452626855CA11GENIChomozygous114550619
135262906052629061TC23GENIChomozygous114550621
135263031352630314GA22GENIChomozygous114550622
135263088652630887CT14GENIChomozygous114550623
135263091152630912TC17GENIChomozygous114550624
135263107352631074CT18GENIChomozygous114550625
135263136752631368AG12GENIChomozygous114550626
135263136952631370GA10GENIChomozygous114550627
135263152352631524GA14GENIChomozygous114617560
135263152752631528GC14GENIChomozygous114550628
135263158152631582CT23GENIChomozygous114550629
135263190552631906TC18GENIChomozygous114550630
135263204252632043CT21GENIChomozygous114550631
135263255952632560TC15GENIChomozygous114617562
135263288152632882TC15GENICpossibly homozygous114550632
135263334652633347CT32GENIChomozygous114550633
135263342852633429TG22GENIChomozygous114550634
135263351552633516GA22GENIChomozygous114550635
135263400952634010CT14GENIChomozygous114550636
135263412252634123GA16GENIChomozygous114550637
135263414252634143AG12GENIChomozygous114550638
135263415552634156CT16GENIChomozygous114550639
135263417752634178TG13GENIChomozygous114550640
135263423752634238AG16GENIChomozygous114550641
135263476052634761TA24GENIChomozygous114550642
135263608252636083TC20GENIChomozygous114550644
135263675252636753TC20GENIChomozygous114550645
135263688252636883AG13GENIChomozygous114550646