chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162038775920387760GA24GENIChomozygous111948584
162038849920388500AT16GENIChomozygous111948586
162038893920388940CG18GENIChomozygous112107993
162038901220389013TG16GENIChomozygous111752732
162039001420390015CA40GENIChomozygous111948588
162039103420391035TC12GENIChomozygous112052871
162039290620392907TC29GENIChomozygous111752736
162039408120394082GA14GENIChomozygous111948594
162039664820396649TC16GENIChomozygous111752740
162039669120396692TC21GENIChomozygous111752742
162039869620398697CT32GENIChomozygous111948596
162039901720399018TC23GENIChomozygous111948598
162039937020399371GA39GENICpossibly homozygous111948600
162040086520400866GT31GENIChomozygous111948602
162040086720400868AT30GENIChomozygous111948604
162040295620402957TC31GENIChomozygous111752748
162040368420403685CT28GENIChomozygous111948606
162040395720403958AG27GENIChomozygous111752752
162040425120404252AG47GENIChomozygous111948608
162040438020404381GA36GENIChomozygous111948610
162040509020405091CT31GENIChomozygous111948612
162040553120405532GA25GENIChomozygous111752758
162040861520408616CT37GENIChomozygous111948614
162040865420408655GA33GENIChomozygous111948616
162040865720408658GA34GENIChomozygous111948618
162040885420408855AG49GENIChomozygous111948620
162040890520408906AG47GENIChomozygous111752762
162041153220411533CT36GENIChomozygous111948622
162041234120412342CT29GENIChomozygous111948624
162041243920412440CT34GENIChomozygous111948626
162041265020412651AG34GENIChomozygous111752778
162041287620412877AG31GENIChomozygous111752780
162041290120412902GT28GENIChomozygous111948628
162041310520413106AG27GENIChomozygous111752782
162041358920413590GA31GENIChomozygous111948630
162041359120413592GA32GENIChomozygous111752786