chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159681856396818564CG45GENICpossibly homozygous112604091
159681908596819086TC31GENIChomozygous118931658
159681909496819095GC29GENIChomozygous118931659
159681909796819098GC27GENIChomozygous118931660
159681910196819102GC26GENIChomozygous118931661
159681911096819111TC27GENIChomozygous118931662
159681911596819116TC26GENIChomozygous118931663
159681912496819125TC23GENIChomozygous118931664
159681913596819136TC5GENIChomozygous118931665
159681913896819139TC5GENIChomozygous118931666
159681952696819527TG38GENIChomozygous112604093
159682143096821431TG57GENICpossibly homozygous112756035
159682036796820368TG56GENIChomozygous112756031
159682070196820702GA61GENIChomozygous112756033
159682453996824540TC50GENIChomozygous112604101