chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101288604101288605TG54GENIChomozygous116983364
10101289526101289527G14GENIChomozygous128853913
10101289557101289557CG13GENIChomozygous132694547
10101289562101289562CC13GENIChomozygous132694548
10101289563101289563A13GENIChomozygous132694549
10101289565101289566TA12GENIChomozygous116709437
10101289574101289575AT13GENIChomozygous116709439
10101290387101290388G22GENIChomozygous128853916
10101290392101290392C22GENIChomozygous128853917
10101291337101291338GT46GENIChomozygous116983366
10101292625101292637AGAAAGAGAGAA31GENIChomozygous132694550
10101292743101292743AT39GENICpossibly homozygous131097671
10101293093101293094T42GENIChomozygous132694551
10101293612101293613TC41GENIChomozygous116957901