chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10111032453111032454GC41GENIChomozygous117036208
10111032649111032650CT28GENIChomozygous117297759
10111033349111033350TG30GENIChomozygous117297761
10111035068111035069AG30GENIChomozygous116721350
10111036975111036976TC11GENICpossibly homozygous116721356
10111037954111037955TC30GENIChomozygous116721358
10111038040111038041CT20GENIChomozygous117297763
10111041249111041250AG27GENIChomozygous116721360
10111041699111041700TC27GENIChomozygous116721364
10111042267111042268AG20GENIChomozygous116721368