chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166915950166915951AG33GENIChomozygous108357315
1166916645166916646TC50GENIChomozygous108357316
1166917759166917760AT14GENIChomozygous108357317
1166918446166918447GA48GENIChomozygous108357318
1166922282166922283AG48GENIChomozygous108357319
1166925744166925745AG31GENIChomozygous108357320
1166925756166925757GA31GENIChomozygous108357321
1166928994166928995TA32GENICpossibly homozygous108357322
1166929701166929702CG53GENIChomozygous108357323
1166931260166931261CT51GENICpossibly homozygous108357324
1166931979166931980TC43GENIChomozygous108357325
1166932505166932506GT37GENIChomozygous108357326