chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151379472151379473TG19GENICheterozygous113244162
4151379473151379474AG18GENICheterozygous119454993
4151380115151380116TC8GENIChomozygous112886010
4151388655151388656TC14GENIChomozygous112886012
4151391132151391133AC8GENIChomozygous112886013
4151391175151391176CT19GENIChomozygous112886014
4151391761151391762GA12GENIChomozygous112886015
4151394598151394599GA6GENIChomozygous112886016
4151395043151395044CT4GENIChomozygous112886017
4151395187151395188TC9GENIChomozygous112886018
4151395515151395516AG14GENIChomozygous112886019
4151395953151395954TC6GENIChomozygous112886020
4151396190151396191TA12GENIChomozygous112886021
4151396252151396253GT10GENIChomozygous112886022
4151396579151396580GC9GENIChomozygous112886023