chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151380115151380116TC43GENIChomozygous112886010
4151382963151382964GA46GENICheterozygous112886011
4151388655151388656TC89GENIChomozygous112886012
4151391132151391133AC54GENIChomozygous112886013
4151391175151391176CT55GENIChomozygous112886014
4151391761151391762GA55GENIChomozygous112886015
4151394598151394599GA50GENIChomozygous112886016
4151395043151395044CT60GENIChomozygous112886017
4151395187151395188TC53GENIChomozygous112886018
4151395515151395516AG68GENIChomozygous112886019
4151395953151395954TC45GENIChomozygous112886020
4151396190151396191TA51GENIChomozygous112886021
4151396252151396253GT50GENIChomozygous112886022
4151396579151396580GC43GENIChomozygous112886023